Variant #0000946935 (NC_000001.10:g.1148414G>A, NM_016176.3:c.*4478C>T (SDF4))

Chromosome 1
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.1148414G>A
DNA change (hg38) -
Published as TNFRSF4(NM_003327.4):c.328C>T (p.R110W)
ISCN -
DB-ID SDF4_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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF4 NM_003327.3 ?/. - c.328C>T r.(?) p.(Arg110Trp)
SDF4 NM_016176.3 ?/. - c.*4478C>T r.(=) p.(=)


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