Variant #0000724152 (NC_000012.11:g.57145980C>A, NM_000946.2:c.103G>T (PRIM1))

Chromosome 12
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.57145980C>A
DNA change (hg38) -
Published as PRIM1(NM_000946.3):c.103G>T (p.V35L)
ISCN -
DB-ID HSD17B6_000001
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PRIM1 NM_000946.2 ?/. - c.103G>T r.(?) p.(Val35Leu)
HSD17B6 NM_003725.2 ?/. - c.-11238C>A r.(?) p.(=)


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