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Chr Start Stop Change Gene(s) HGVS_C HGVS_P Sample Count CMH MAF ACMG Cat. ACMG Note Curation
View 1 977028 977028 G > T AGRN NM_198576.3:c.1123G>T
NP_940978.2:p.Ala375Ser
100/9594 0.00532 4 non_synonymous Likely Benign
View 1 978974 978974 G > A AGRN NM_198576.3:c.1660G>A
NP_940978.2:p.Val554Met
93/9594 0.00485 4 Common ExAC MAF original cat: TYPE_3 - non_synonymous Likely Benign
View 1 981942 981942 C > A AGRN NM_198576.3:c.3077C>A
NP_940978.2:p.Thr1026Asn
92/9594 0.00479 4 Common ExAC MAF original cat: TYPE_3 - non_synonymous Likely Benign
View 1 982213 982213 G > C AGRN NM_198576.3:c.3264G>C
NP_940978.2:p.Leu1088Phe
187/9594 0.00975 4 Common ExAC MAF original cat: TYPE_3 - non_synonymous Likely Benign
View 1 984971 984971 G > A AGRN NM_198576.3:c.4540G>A
NP_940978.2:p.Ala1514Thr
191/9594 0.00995 4 non_synonymous Likely Benign
View 1 1273790 1273790 T > C DVL1 NM_004421.2:c.1291A>G
NP_004412.2:p.Thr431Ala
61/9594 0.00318 4 non_synonymous Likely Benign
View 1 1277040 1277041 CA > - DVL1 NM_004421.2:c.605+6_605+7del
33/9594 0.00172 3 five_prime_flank Likely Benign
View 1 1961512 1961512 C > T GABRD NM_000815.4:c.1150C>T
NP_000806.2:p.Pro384Ser
13/9594 0.00068 4 non_synonymous Likely Benign
View 1 2234791 2234791 C > T SKI NM_003036.3:c.1163C>T
NP_003027.1:p.Ala388Val
113/9594 0.00589 4 Likely Benign
View 1 2234824 2234824 C > T SKI NM_003036.3:c.1196C>T
NP_003027.1:p.Ala399Val
9/9594 0.00047 4 non_synonymous Likely Benign
View 1 2338250 2338250 C > G PEX10 PEX10 NM_153818.1:c.745G>C
NM_002617.3:c.685G>C
NP_722540.1:p.Val249Leu
NP_002608.1:p.Val229Leu
50/11422 0.00228 4 Common ExAC MAF original cat: TYPE_3 - non_synonymous Likely Benign
View 1 3329051 3329051 G > A PRDM16 PRDM16 NM_199454.2:c.2290G>A
NM_022114.3:c.2290G>A
NP_955533.2:p.Val764Met
NP_071397.3:p.Val764Met
35/9594 0.00182 4 non_synonymous Likely Benign
View 1 5935064 5935064 T > C NPHP4 NM_015102.3:c.2914A>G
NP_055917.1:p.Ser972Gly
55/11422 0.00241 4 Likely Benign
View 1 5965750 5965750 G > C NPHP4 NM_015102.3:c.1705C>G
NP_055917.1:p.Gln569Glu
32/11422 0.0014 4 Likely Benign
View 1 6027365 6027365 C > T NPHP4 NM_015102.3:c.511G>A
NP_055917.1:p.Ala171Thr
32/11422 0.0014 4 Likely Benign
View 1 6504654 6504654 T > G ESPN NM_031475.2:c.1104T>G
NP_113663.2:p.Phe368Leu
19/9594 0.00099 4 non_synonymous Likely Benign
View 1 7724562 7724562 C > T CAMTA1 NM_015215.2:c.1955C>T
NP_056030.1:p.Ser652Leu
46/9594 0.00245 4 non_synonymous Likely Benign
View 1 7792679 7792679 C > T CAMTA1 NM_015215.2:c.3066+20C>T
20/9555 0.00105 4 five_prime_intronic Likely Benign
View 1 8415618 8415618 G > T RERE RERE RERE NM_012102.3:c.4528C>A
NM_001042682.1:c.2866C>A
NM_001042681.1:c.4528C>A
NP_036234.3:p.Pro1510Thr
NP_001036147.1:p.Pro956Thr
NP_001036146.1:p.Pro1510Thr
45/9594 0.00235 4 non_synonymous Likely Benign
View 1 8420065 8420065 C > A RERE RERE RERE NM_012102.3:c.3396-19G>T
NM_001042682.1:c.1734-19G>T
NM_001042681.1:c.3396-19G>T
3/9555 0.00016 4 three_prime_flank Likely Benign
View 1 8421096 8421096 G > A RERE RERE RERE NM_012102.3:c.2471C>T
NM_001042682.1:c.809C>T
NM_001042681.1:c.2471C>T
NP_036234.3:p.Pro824Leu
NP_001036147.1:p.Pro270Leu
NP_001036146.1:p.Pro824Leu
7/9594 0.00036 4 non_synonymous Likely Benign
View 1 8421875 8421875 G > A RERE RERE RERE NM_012102.3:c.1964C>T
NM_001042682.1:c.302C>T
NM_001042681.1:c.1964C>T
NP_036234.3:p.Ala655Val
NP_001036147.1:p.Ala101Val
NP_001036146.1:p.Ala655Val
15/9594 0.00078 4 non_synonymous Likely Benign
View 1 8568666 8568666 G > A RERE RERE NM_012102.3:c.879+20C>T
NM_001042681.1:c.879+20C>T
68/9555 0.00361 4 Common ExAC MAF original cat: TYPE_3 - five_prime_intronic Likely Benign
View 1 8616562 8616562 C > T RERE RERE NM_012102.3:c.697G>A
NM_001042681.1:c.697G>A
NP_036234.3:p.Val233Ile
NP_001036146.1:p.Val233Ile
15/9594 0.00078 4 non_synonymous Likely Benign
View 1 8716321 8716322 - > TCTTTG RERE RERE NM_012102.3:c.30_35dupCAAAGA
NM_001042681.1:c.30_35dupCAAAGA
NP_036234.3:p.Asp10_Lys11dup
NP_001036146.1:p.Asp10_Lys11dup
11/9594 0.00057 4 in_frame_indel Likely Benign
View 1 10032249 10032249 A > G NMNAT1 NM_022787.3:c.115+3A>G
108/9594 0.00578 4 Likely Benign
View 1 10364260 10364260 A > G KIF1B KIF1B NM_015074.3:c.1977+6956A>G
NM_183416.3:c.3017A>G
NP_904325.2:p.Glu1006Gly
84/9594 0.00438 4 non_synonymous Likely Benign
View 1 10436626 10436626 C > T KIF1B NM_015074.3:c.5294C>T
NP_055889.2:p.Pro1765Leu
91/9594 0.00474 4 non_synonymous Likely Benign
View 1 11105542 11105542 C > T MASP2 MASP2 NM_006610.3:c.467G>A
NM_139208.2:c.467G>A
NP_006601.2:p.Cys156Tyr
NP_631947.1:p.Cys156Tyr
128/9594 0.00672 4 Likely Benign
View 1 11291348 11291348 G > A MTOR NM_004958.3:c.2649+9C>T
16/9594 0.00083 4 five_prime_intronic Likely Benign
View 1 11907430 11907430 T > G NPPA NPPA-AS1 NM_006172.3:c.190A>C
NR_037806.1:n.1480-61T>G
NP_006163.1:p.Ser64Arg
44/9594 0.00229 4 Likely Benign
View 1 17355075 17355075 A > T SDHB TRNAN-GUU NM_003000.2:c.423+20T>A
52/9555 0.00277 4 Likely Benign
View 1 17371286 17371286 T > C SDHB TRNAN-GUU NM_003000.2:c.170A>G
NP_002991.2:p.His57Arg
17/9594 0.00089 4 Likely Benign
View 1 19566858 19566858 G > A EMC1 TRNAN-GUU EMC1 EMC1 EMC1 NM_015047.2:c.719C>T
NM_001271427.1:c.719C>T
NM_001271428.1:c.719C>T
NM_001271429.1:c.653C>T
NP_055862.1:p.Pro240Leu
NP_001258356.1:p.Pro240Leu
NP_001258357.1:p.Pro240Leu
NP_001258358.1:p.Pro218Leu
37/9594 0.00193 4 non_synonymous Likely Benign
View 1 21554554 21554554 A > C ECE1 TRNAN-GUU ECE1 ECE1 ECE1 NM_001397.2:c.1671-20T>G
NM_001113347.1:c.1635-20T>G
NM_001113349.1:c.1662-20T>G
NM_001113348.1:c.1623-20T>G
136/9556 0.00712 4 three_prime_flank Likely Benign
View 1 21564631 21564631 C > T ECE1 TRNAN-GUU ECE1 ECE1 ECE1 NM_001397.2:c.1385G>A
NM_001113347.1:c.1349G>A
NM_001113349.1:c.1376G>A
NM_001113348.1:c.1337G>A
NP_001388.1:p.Ser462Asn
NP_001106818.1:p.Ser450Asn
NP_001106820.1:p.Ser459Asn
NP_001106819.1:p.Ser446Asn
95/9594 0.00495 4 non_synonymous Likely Benign
View 1 21903947 21903947 G > A TRNAN-GUU ALPL ALPL ALPL ENST00000374840.3:c.1381G>A
ENST00000539907.1:c.1150G>A
ENST00000540617.1:c.1216G>A
ENSP00000363973.3:p.Val461Ile
ENSP00000437674.1:p.Val384Ile
ENSP00000442672.1:p.Val406Ile
56/11422 0.00245 4 Likely Benign
View 1 22155561 22155561 G > C TRNAN-GUU HSPG2 NM_005529.5:c.12004C>G
NP_005520.4:p.Leu4002Val
19/11422 0.00083 4 non_synonymous Likely Benign
View 1 22161190 22161190 C > T TRNAN-GUU HSPG2 NM_005529.5:c.10702G>A
NP_005520.4:p.Val3568Ile
73/11422 0.00324 4 Common ExAC MAF original cat: TYPE_3 - non_synonymous Likely Benign
View 1 22161394 22161394 C > T TRNAN-GUU HSPG2 NM_005529.5:c.10498G>A
NP_005520.4:p.Val3500Met
99/11422 0.00438 4 non_synonymous Likely Benign
View 1 22166034 22166034 G > A TRNAN-GUU HSPG2 NM_005529.5:c.9719C>T
NP_005520.4:p.Ala3240Val
79/11422 0.00346 4 Common ExAC MAF original cat: TYPE_3 - non_synonymous Likely Benign
View 1 22205601 22205601 T > C TRNAN-GUU HSPG2 NM_005529.5:c.2357A>G
NP_005520.4:p.Asn786Ser
102/11422 0.00447 4 non_synonymous Likely Benign
View 1 24019079 24019079 G > T TRNAN-GUU RPL11 RPL11 NM_001199802.1:c.7-23G>T
NM_000975.3:c.7-20G>T
73/9555 0.00382 4 three_prime_flank Likely Benign
View 1 24123348 24123348 C > T GALE TRNAN-GUU GALE GALE NM_001008216.1:c.709+18G>A
NM_000403.3:c.709+18G>A
NM_001127621.1:c.709+18G>A
40/9555 0.00215 4 five_prime_intronic Likely Benign
View 1 24181041 24181041 C > T TRNAN-GUU FUCA1 NM_000147.4:c.778G>A
NP_000138.2:p.Val260Ile
16/11422 0.0007 4 non_synonymous Likely Benign
View 1 24194770 24194770 C > G TRNAN-GUU FUCA1 NM_000147.4:c.7G>C
NP_000138.2:p.Ala3Pro
261/11422 0.01186 4 non_synonymous Likely Benign
View 1 24687371 24687371 C > T STPG1 STPG1 STPG1 GRHL3 TRNAN-GUU STPG1 NM_001199013.1:c.898G>A
NM_001199012.1:c.898G>A
NM_178122.4:c.757G>A
NM_198174.2:c.1695-3304C>T
NM_001199014.1:c.622G>A
NP_001185942.1:p.Ala300Thr
NP_001185941.1:p.Ala300Thr
NP_835223.1:p.Ala253Thr
NP_001185943.1:p.Ala208Thr
113/9555 0.00602 4 non_synonymous Likely Benign
View 1 27023366 27023366 C > T ARID1A TRNAN-GUU ARID1A NM_139135.2:c.472C>T
NM_006015.4:c.472C>T
NP_624361.1:p.Pro158Ser
NP_006006.3:p.Pro158Ser
36/9594 0.00198 4 non_synonymous Likely Benign
View 1 27023759 27023759 C > T ARID1A TRNAN-GUU ARID1A NM_139135.2:c.865C>T
NM_006015.4:c.865C>T
NP_624361.1:p.Pro289Ser
NP_006006.3:p.Pro289Ser
4/9594 0.00021 4 non_synonymous Likely Benign
View 1 27087500 27087500 A > G ARID1A TRNAN-GUU ARID1A NM_139135.2:c.2074A>G
NM_006015.4:c.2074A>G
NP_624361.1:p.Ile692Val
NP_006006.3:p.Ile692Val
4/9594 0.00021 4 Likely Benign
Displaying 1 through 50 of 2,802 variants