Variant #0000274393 (NC_000009.11:g.126125186C>T, NM_173689.5:c.137C>T (CRB2))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.126125186C>T
DNA change (hg38) g.123362907C>T
Published as CRB2(NM_173689.5):c.137C>T (p.(Pro46Leu)), CRB2(NM_173689.6):c.137C>T (p.P46L), CRB2(NM_173689.7):c.137C>T (p.P46L)
ISCN -
DB-ID CRB2_000017 See all 3 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) 0.00212 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRB2 NM_173689.5 -/. - c.137C>T r.(?) p.(Pro46Leu)


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