Linked Data
ClinVar Variation Id:
89338
ClinVar RCV Id:
RCV000074803
RCV000223452
RCV000484829
RCV000524153
RCV001355855
RCV001194362
RCV002477211
RCV003450957
RCV003162473
dbSNP Id:
rs63749999
ExAC:
2:48028225 C / T
gnomAD v2:
2-48028225-C-T
gnomAD v4:
2-47801086-C-T
COSMIC:
COSM5451671
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47801086C>T , CM000664.2:g.47801086C>T | GRCh38 |
| NC_000002.11:g.48028225C>T , CM000664.1:g.48028225C>T | GRCh37 |
| NC_000002.10:g.47881729C>T | NCBI36 |
| NG_007111.1:g.22940C>T , LRG_219:g.22940C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.2806C>T (MSH6) | ENSP00000406248.2:p.Arg936Ter | |
| ENST00000420813.6:c.2806C>T (MSH6) | ENSP00000390382.2:p.Arg936Ter | |
| ENST00000455383.6:c.2806C>T (MSH6) | ENSP00000397484.2:p.Arg936Ter | |
| ENST00000700004.2:c.3103C>T (MSH6) | ENSP00000514752.2:p.Arg1035Ter | |
| ENST00000699999.1:n.3187C>T (MSH6) | ||
| ENST00000700000.1:c.1606+1497C>T (MSH6) | ENSP00000514749.1:n.1606+1497C>T | |
| ENST00000700002.1:c.3109C>T (MSH6) | ENSP00000514750.1:p.Arg1037Ter | |
| ENST00000700003.1:c.628-2334C>T (MSH6) | ENSP00000514751.1:n.628-2334C>T | |
| ENST00000700004.1:c.2260C>T (MSH6) | ENSP00000514752.1:p.Arg754Ter | |
| ENST00000234420.11:c.3103C>T (MSH6) MANE Select | ENSP00000234420.5:p.Arg1035Ter | |
| ENST00000540021.6:c.2713C>T (MSH6) | ENSP00000446475.1:p.Arg905Ter | |
| ENST00000652107.1:c.2806C>T (MSH6) | ENSP00000498629.1:p.Arg936Ter | |
| ENST00000673637.1:c.2806C>T (MSH6) | ENSP00000501310.1:p.Arg936Ter | |
| ENST00000234420.9:c.3103C>T (MSH6) | ENSP00000234420.4:p.Arg1035Ter | |
| ENST00000405808.5:c.169+7109G>A (FBXO11) | ENSP00000385127.1:n.169+7109G>A | |
| ENST00000434234.5:c.*124+6908G>A (FBXO11) | ENSP00000402692.1:n.*124+6908G>A | |
| ENST00000445503.5:c.*2450C>T (MSH6) | ENSP00000405294.1:n.*2450C>T | |
| ENST00000538136.1:c.2197C>T (MSH6) | ENSP00000438580.1:p.Arg733Ter | |
| ENST00000540021.5:c.2713C>T (MSH6) | ENSP00000446475.1:p.Arg905Ter | |
| ENST00000614496.4:c.2197C>T (MSH6) | ENSP00000477844.1:p.Arg733Ter | |
| ENST00000616033.4:c.3100C>T (MSH6) | ENSP00000480261.1:p.Arg1034Ter | |
| ENST00000622629.4:c.7C>T (MSH6) | ENSP00000482078.1:p.Arg3Ter | |
| NM_000179.2:c.3103C>T , LRG_219t1:c.3103C>T (MSH6) | NP_000170.1:p.Arg1035Ter | |
| NM_001281492.1:c.2713C>T (MSH6) | NP_001268421.1:p.Arg905Ter | |
| NM_001281493.1:c.2197C>T (MSH6) | NP_001268422.1:p.Arg733Ter | |
| NM_001281494.1:c.2197C>T (MSH6) | NP_001268423.1:p.Arg733Ter | |
| XM_005264271.1:c.2806C>T (MSH6) | XP_005264328.1:p.Arg936Ter | |
| XM_011532798.1:c.2920C>T (MSH6) | XP_011531100.1:p.Arg974Ter | |
| XM_011532799.1:c.2806C>T (MSH6) | XP_011531101.1:p.Arg936Ter | |
| XM_011532800.1:c.2806C>T (MSH6) | XP_011531102.1:p.Arg936Ter | |
| XM_024452819.1:c.3103C>T (MSH6) | XP_024308587.1:p.Arg1035Ter | |
| XM_024452820.1:c.2920C>T (MSH6) | XP_024308588.1:p.Arg974Ter | |
| XM_024452821.1:c.2806C>T (MSH6) | XP_024308589.1:p.Arg936Ter | |
| XM_024452822.1:c.2197C>T (MSH6) | XP_024308590.1:p.Arg733Ter | |
| NM_000179.3:c.3103C>T (MSH6) MANE Select | NP_000170.1:p.Arg1035Ter | |
| NM_001281492.2:c.2713C>T (MSH6) | NP_001268421.1:p.Arg905Ter | |
| NM_001281493.2:c.2197C>T (MSH6) | NP_001268422.1:p.Arg733Ter | |
| NM_001281494.2:c.2197C>T (MSH6) | NP_001268423.1:p.Arg733Ter |