Variant #0000009666 (NC_000003.12:g.37028782A>G, MLH1(NM_000249.4):c.1410-2A>G)
Individual ID |
00002455 |
Chromosome |
3 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.37028782A>G |
Reference |
- |
DB-ID |
MLH1_000081 |
dbSNP ID |
rs746536721 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Pablo Kalfayan-Hospital Italiano |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Variant on transcripts
Screenings
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