Variant #0000621398 (NC_000004.11:g.56233887C>A, NM_024592.4:c.695C>A (SRD5A3))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.56233887C>A
DNA change (hg38) g.55367720C>A
Published as SRD5A3(NM_024592.4):c.695C>A (p.A232E)
ISCN -
DB-ID SRD5A3_000003
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 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SRD5A3 NM_024592.4 -?/. - c.695C>A r.(?) p.(Ala232Glu)
SRD5A3-AS1 NR_037969.1 -?/. - n.364-557G>T r.(?) -


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