Linked Data
ClinVar Variation Id:
89352
ClinVar RCV Id:
RCV000074817
RCV000160692
RCV000201960
RCV000172816
RCV000524156
RCV000607176
RCV000763497
RCV001249973
RCV001253564
RCV001353539
RCV003389678
RCV003162474
dbSNP Id:
rs63749843
gnomAD v3:
2-47803449-C-T
gnomAD v4:
2-47803449-C-T
COSMIC:
COSM6475266
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47803449C>T , CM000664.2:g.47803449C>T | GRCh38 |
| NC_000002.11:g.48030588C>T , CM000664.1:g.48030588C>T | GRCh37 |
| NC_000002.10:g.47884092C>T | NCBI36 |
| NG_007111.1:g.25303C>T , LRG_219:g.25303C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.2905C>T (MSH6) | ENSP00000406248.2:p.Arg969Ter | |
| ENST00000420813.6:c.2905C>T (MSH6) | ENSP00000390382.2:p.Arg969Ter | |
| ENST00000455383.6:c.2905C>T (MSH6) | ENSP00000397484.2:p.Arg969Ter | |
| ENST00000700004.2:c.3173-2169C>T (MSH6) | ENSP00000514752.2:n.3173-2169C>T | |
| ENST00000699999.1:n.3286C>T (MSH6) | ||
| ENST00000700000.1:c.1636C>T (MSH6) | ENSP00000514749.1:p.Arg546Ter | |
| ENST00000700002.1:c.3208C>T (MSH6) | ENSP00000514750.1:p.Arg1070Ter | |
| ENST00000700003.1:c.657C>T (MSH6) | ENSP00000514751.1:p.Val219= | |
| ENST00000700004.1:c.2330-2169C>T (MSH6) | ENSP00000514752.1:n.2330-2169C>T | |
| ENST00000700005.1:n.2053C>T (MSH6) | ||
| ENST00000700006.1:n.2050C>T (MSH6) | ||
| ENST00000700007.1:n.1207C>T (MSH6) | ||
| ENST00000700008.1:n.781C>T (MSH6) | ||
| ENST00000700009.1:n.780C>T (MSH6) | ||
| ENST00000700010.1:n.611C>T (MSH6) | ||
| ENST00000700011.1:n.682C>T (MSH6) | ||
| ENST00000234420.11:c.3202C>T (MSH6) MANE Select | ENSP00000234420.5:p.Arg1068Ter | |
| ENST00000540021.6:c.2812C>T (MSH6) | ENSP00000446475.1:p.Arg938Ter | |
| ENST00000652107.1:c.2905C>T (MSH6) | ENSP00000498629.1:p.Arg969Ter | |
| ENST00000673637.1:c.2905C>T (MSH6) | ENSP00000501310.1:p.Arg969Ter | |
| ENST00000234420.9:c.3202C>T (MSH6) | ENSP00000234420.4:p.Arg1068Ter | |
| ENST00000405808.5:c.169+4746G>A (FBXO11) | ENSP00000385127.1:n.169+4746G>A | |
| ENST00000434234.5:c.*124+4545G>A (FBXO11) | ENSP00000402692.1:n.*124+4545G>A | |
| ENST00000445503.5:c.*2549C>T (MSH6) | ENSP00000405294.1:n.*2549C>T | |
| ENST00000538136.1:c.2296C>T (MSH6) | ENSP00000438580.1:p.Arg766Ter | |
| ENST00000540021.5:c.2812C>T (MSH6) | ENSP00000446475.1:p.Arg938Ter | |
| ENST00000614496.4:c.2296C>T (MSH6) | ENSP00000477844.1:p.Arg766Ter | |
| ENST00000622629.4:c.106C>T (MSH6) | ENSP00000482078.1:p.Arg36Ter | |
| NM_000179.2:c.3202C>T , LRG_219t1:c.3202C>T (MSH6) | NP_000170.1:p.Arg1068Ter | |
| NM_001281492.1:c.2812C>T (MSH6) | NP_001268421.1:p.Arg938Ter | |
| NM_001281493.1:c.2296C>T (MSH6) | NP_001268422.1:p.Arg766Ter | |
| NM_001281494.1:c.2296C>T (MSH6) | NP_001268423.1:p.Arg766Ter | |
| XM_005264271.1:c.2905C>T (MSH6) | XP_005264328.1:p.Arg969Ter | |
| XM_011532798.1:c.3019C>T (MSH6) | XP_011531100.1:p.Arg1007Ter | |
| XM_011532799.1:c.2905C>T (MSH6) | XP_011531101.1:p.Arg969Ter | |
| XM_011532800.1:c.2905C>T (MSH6) | XP_011531102.1:p.Arg969Ter | |
| XM_024452819.1:c.3202C>T (MSH6) | XP_024308587.1:p.Arg1068Ter | |
| XM_024452820.1:c.3019C>T (MSH6) | XP_024308588.1:p.Arg1007Ter | |
| XM_024452821.1:c.2905C>T (MSH6) | XP_024308589.1:p.Arg969Ter | |
| XM_024452822.1:c.2296C>T (MSH6) | XP_024308590.1:p.Arg766Ter | |
| NM_000179.3:c.3202C>T (MSH6) MANE Select | NP_000170.1:p.Arg1068Ter | |
| NM_001281492.2:c.2812C>T (MSH6) | NP_001268421.1:p.Arg938Ter | |
| NM_001281493.2:c.2296C>T (MSH6) | NP_001268422.1:p.Arg766Ter | |
| NM_001281494.2:c.2296C>T (MSH6) | NP_001268423.1:p.Arg766Ter |