Variant #0000502567 (NC_000001.10:g.1147337C>T, NM_016176.3:c.*5555G>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.1147337C>T
DNA change (hg38) g.1211957C>T
Published as TNFRSF4(NM_003327.4):c.619G>A (p.V207M)
ISCN -
DB-ID SDF4_000003 See all 2 reported entries
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) 0.00085 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF4 NM_003327.3 -?/. - c.619G>A r.(?) p.(Val207Met)
SDF4 NM_016176.3 -?/. - c.*5555G>A r.(=) p.(=)


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