Variant #0000147866 (NC_000011.9:g.88911127C>T, NM_000372.4:c.6C>T (TYR))
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.88911127C>T |
DNA change (hg38) |
g.89177959C>T |
Published as |
- |
ISCN |
- |
DB-ID |
TYR_000285 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs35541275 |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
William (Bill) Oetting |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2016-12-03 15:10:32 +01:00 (CET) |
Date last edited |
2016-12-03 15:58:40 +01:00 (CET) |

Variant on transcripts
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