Variant #0000265000 (NC_000001.10:g.197297979_197297987del, NM_201253.2:c.498_506del (CRB1))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.197297979_197297987del |
DNA change (hg38) |
g.197328849_197328857del |
Published as |
CRB1(NM_001257965.1):c.291_299delAATTGATGG (p.I98_G100del), CRB1(NM_001257965.2):c.291_299delAATTGATGG (p.I98_G100del) |
ISCN |
- |
DB-ID |
CRB1_000211 See all 71 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) |
Retrieve |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-09-27 19:20:11 +02:00 (CEST) |

Variant on transcripts
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