Variant #0000851476 (NC_000007.13:g.137782606_137782608del, NC_000007.13(NM_005989.3):c.379-6_379-4del (AKR1D1))

Chromosome 7
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.137782606_137782608del
DNA change (hg38) -
Published as AKR1D1(NM_005989.4):c.379-6_379-4delTTT
ISCN -
DB-ID AKR1D1_000009
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AKR1D1 NM_005989.3 -/. - c.379-6_379-4del r.spl? p.?


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