Variant #0000504686 (NC_000001.10:g.197396689C>T, NM_201253.2:c.2234C>T (CRB1))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.197396689C>T |
DNA change (hg38) |
g.197427559C>T |
Published as |
CRB1(NM_001257965.1):c.2027C>T (p.T676M), CRB1(NM_001257965.2):c.2027C>T (p.T676M) |
ISCN |
- |
DB-ID |
CRB1_000021 See all 80 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
7.0E-5 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2021-02-08 18:36:18 +01:00 (CET) |

Variant on transcripts
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