Variant #0000320411 (NC_000001.10:g.1153129C>T, NC_000001.10(NM_016176.3):c.913-61G>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.1153129C>T
DNA change (hg38) g.1217749C>T
Published as SDF4(NM_016547.3):c.947G>A (p.(Arg316Gln))
ISCN -
DB-ID SDF4_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) 0.0013 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.-3622G>A r.(?) p.(=)
SDF4 NM_016176.3 -?/. - c.913-61G>A r.(=) p.(=)


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