Variant #0000504673 (NC_000001.10:g.197168819_197168823del, NM_201253.2:c.-68724_-68720del (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.197168819_197168823del
DNA change (hg38) g.197199689_197199693del
Published as ZBTB41(NM_194314.2):c.784_788del (p.(Lys262Ter))
ISCN -
DB-ID CRB1_000296
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-10-29 20:49:11 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZBTB41 NM_194314.2 ?/. - c.784_788del r.(?) p.(Lys262Ter)
CRB1 NM_201253.2 ?/. - c.-68724_-68720del r.(?) p.(=)


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