Variant #0000856889 (NC_000001.10:g.1149477C>T, NM_016176.3:c.*3415G>A (SDF4))

Chromosome 1
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.1149477C>T
DNA change (hg38) -
Published as TNFRSF4(NM_003327.4):c.31G>A (p.G11R)
ISCN -
DB-ID SDF4_000008
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) 0.0001 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +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     
TNFRSF4 NM_003327.3 -?/. - c.31G>A r.(?) p.(Gly11Arg)
SDF4 NM_016176.3 -?/. - c.*3415G>A r.(=) p.(=)


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