ClinVar Variation:
COSMIC:
COSM5021444
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.94740858 (EAS)
Genomes Max Group AF
0.91109495 (EAS)
Exomes Max Group AF
0.94974276 (EAS)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.6300980C>T , CM000666.2:g.6300980C>T | GRCh38 |
| NC_000004.11:g.6302707C>T , CM000666.1:g.6302707C>T | GRCh37 |
| NC_000004.10:g.6353608C>T | NCBI36 |
| NG_011700.1:g.36131C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682275.1:c.1221C>T | ENSP00000507852.1:p.Val407= | |
| ENST00000683395.1:c.1162C>T | ||
| ENST00000684087.1:c.1185C>T | ENSP00000506978.1:p.Val395= | |
| ENST00000506362.2:c.936C>T | ENSP00000424103.2:p.Val312= | |
| ENST00000673642.1:c.844C>T | ENSP00000501242.1:p.Gln282Ter | |
| ENST00000673991.1:c.1221C>T | ENSP00000501033.1:p.Val407= | |
| ENST00000226760.5:c.1185C>T MANE Select | ENSP00000226760.1:p.Val395= | |
| ENST00000503569.5:c.1185C>T | ENSP00000423337.1:p.Val395= | |
| ENST00000507765.1:n.1370C>T | ||
| NM_001145853.1:c.1185C>T | NP_001139325.1:p.Val395= | |
| NM_006005.3:c.1185C>T MANE Select | NP_005996.2:p.Val395= | |
| XM_017008586.1:c.1194C>T | XP_016864075.1:p.Val398= |