Variant #0000515685 (NC_000002.11:g.31751174_31751175insATATATATATATATATAT, NM_000348.3:c.*91_*92insATATATATATATATATAT (SRD5A2))

Chromosome 2
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.31751174_31751175insATATATATATATATATAT
DNA change (hg38) g.31526104_31526105insATATATATATATATATAT
Published as SRD5A2(NM_000348.3):c.*91_*92insATATATATATATATATAT
ISCN -
DB-ID SRD5A2_000100
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRD5A2 NM_000348.3 -/. - c.*91_*92insATATATATATATATATAT r.(=) p.(=)


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