Variant #0000979857 (NC_000011.9:g.71164364G>A, NM_001360.2:c.-5160C>T (DHCR7))

Chromosome 11
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.71164364G>A
DNA change (hg38) -
Published as NADSYN1(NM_018161.5):c.22G>A (p.(Ala8Thr))
ISCN -
DB-ID DHCR7_000293
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) 0.00023 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     

Haplotype     
DHCR7 NM_001360.2 ?/. - c.-5160C>T r.(?) p.(=) -
NADSYN1 NM_018161.4 ?/. - c.22G>A r.(?) p.(Ala8Thr) -


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