Linked Data
ClinVar Variation Id:
141274
dbSNP Id:
rs63750442
ExAC:
2:48030685 C / G
gnomAD v2:
2-48030685-C-G
gnomAD v3:
2-47803546-C-G
gnomAD v4:
2-47803546-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.47803546C>G , CM000664.2:g.47803546C>G | GRCh38 |
| NC_000002.11:g.48030685C>G , CM000664.1:g.48030685C>G | GRCh37 |
| NC_000002.10:g.47884189C>G | NCBI36 |
| NG_007111.1:g.25400C>G , LRG_219:g.25400C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000411819.2:c.3002C>G (MSH6) | ENSP00000406248.2:p.Thr1001Arg | |
| ENST00000420813.6:c.3002C>G (MSH6) | ENSP00000390382.2:p.Thr1001Arg | |
| ENST00000455383.6:c.3002C>G (MSH6) | ENSP00000397484.2:p.Thr1001Arg | |
| ENST00000700004.2:c.3173-2072C>G (MSH6) | ENSP00000514752.2:n.3173-2072C>G | |
| ENST00000699999.1:n.3383C>G (MSH6) | ||
| ENST00000700000.1:c.1733C>G (MSH6) | ENSP00000514749.1:p.Thr578Arg | |
| ENST00000700002.1:c.3305C>G (MSH6) | ENSP00000514750.1:p.Thr1102Arg | |
| ENST00000700003.1:c.754C>G (MSH6) | ENSP00000514751.1:n.754C>G | |
| ENST00000700004.1:c.2330-2072C>G (MSH6) | ENSP00000514752.1:n.2330-2072C>G | |
| ENST00000700005.1:n.2150C>G (MSH6) | ||
| ENST00000700006.1:n.2147C>G (MSH6) | ||
| ENST00000700007.1:n.1304C>G (MSH6) | ||
| ENST00000700008.1:n.878C>G (MSH6) | ||
| ENST00000700009.1:n.877C>G (MSH6) | ||
| ENST00000700010.1:n.708C>G (MSH6) | ||
| ENST00000700011.1:n.779C>G (MSH6) | ||
| ENST00000234420.11:c.3299C>G (MSH6) MANE Select | ENSP00000234420.5:p.Thr1100Arg | |
| ENST00000540021.6:c.2909C>G (MSH6) | ENSP00000446475.1:p.Thr970Arg | |
| ENST00000652107.1:c.3002C>G (MSH6) | ENSP00000498629.1:p.Thr1001Arg | |
| ENST00000673637.1:c.3002C>G (MSH6) | ENSP00000501310.1:p.Thr1001Arg | |
| ENST00000234420.9:c.3299C>G (MSH6) | ENSP00000234420.4:p.Thr1100Arg | |
| ENST00000405808.5:c.169+4649G>C (FBXO11) | ENSP00000385127.1:n.169+4649G>C | |
| ENST00000434234.5:c.*124+4448G>C (FBXO11) | ENSP00000402692.1:n.*124+4448G>C | |
| ENST00000445503.5:c.*2646C>G (MSH6) | ENSP00000405294.1:n.*2646C>G | |
| ENST00000538136.1:c.2393C>G (MSH6) | ENSP00000438580.1:p.Thr798Arg | |
| ENST00000540021.5:c.2909C>G (MSH6) | ENSP00000446475.1:p.Thr970Arg | |
| ENST00000614496.4:c.2393C>G (MSH6) | ENSP00000477844.1:p.Thr798Arg | |
| ENST00000622629.4:c.203C>G (MSH6) | ENSP00000482078.1:p.Thr68Arg | |
| NM_000179.2:c.3299C>G , LRG_219t1:c.3299C>G (MSH6) | NP_000170.1:p.Thr1100Arg | |
| NM_001281492.1:c.2909C>G (MSH6) | NP_001268421.1:p.Thr970Arg | |
| NM_001281493.1:c.2393C>G (MSH6) | NP_001268422.1:p.Thr798Arg | |
| NM_001281494.1:c.2393C>G (MSH6) | NP_001268423.1:p.Thr798Arg | |
| XM_005264271.1:c.3002C>G (MSH6) | XP_005264328.1:p.Thr1001Arg | |
| XM_011532798.1:c.3116C>G (MSH6) | XP_011531100.1:p.Thr1039Arg | |
| XM_011532799.1:c.3002C>G (MSH6) | XP_011531101.1:p.Thr1001Arg | |
| XM_011532800.1:c.3002C>G (MSH6) | XP_011531102.1:p.Thr1001Arg | |
| XM_024452819.1:c.3299C>G (MSH6) | XP_024308587.1:p.Thr1100Arg | |
| XM_024452820.1:c.3116C>G (MSH6) | XP_024308588.1:p.Thr1039Arg | |
| XM_024452821.1:c.3002C>G (MSH6) | XP_024308589.1:p.Thr1001Arg | |
| XM_024452822.1:c.2393C>G (MSH6) | XP_024308590.1:p.Thr798Arg | |
| NM_000179.3:c.3299C>G (MSH6) MANE Select | NP_000170.1:p.Thr1100Arg | |
| NM_001281492.2:c.2909C>G (MSH6) | NP_001268421.1:p.Thr970Arg | |
| NM_001281493.2:c.2393C>G (MSH6) | NP_001268422.1:p.Thr798Arg | |
| NM_001281494.2:c.2393C>G (MSH6) | NP_001268423.1:p.Thr798Arg |