Variant #0000147862 (NC_000011.9:g.88911169C>T, NM_000372.4:c.48C>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.88911169C>T |
DNA change (hg38) |
g.89178001C>T |
Published as |
- |
ISCN |
- |
DB-ID |
TYR_000293 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs148710429 |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
3.0E-5 View details |
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 |
2022-10-13 05:07:44 +02:00 (CEST) |

Variant on transcripts
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