Variant #0000008700 (NC_000007.14:g.5982995C>T, NC_000007.14(NM_000535.5):c.2007-4G>A (PMS2))
Individual ID |
00001533 |
Chromosome |
7 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.5982995C>T |
Reference |
- |
DB-ID |
PMS2_000017 See all 12 reported entries |
dbSNP ID |
- |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Dolores Mansilla-Instituto Roffo |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2020-11-08 17:16:06 -02:00 (-02) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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