Variant #0001003361 (NC_000017.10:g.4642637C>T, NM_022059.2:c.55G>A (CXCL16))

Chromosome 17
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.4642637C>T
DNA change (hg38) -
Published as CXCL16(NM_001100812.1):c.55G>A (p.(Glu19Lys))
ISCN -
DB-ID CXCL16_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) 0.0007 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 2024-08-28 13:16:32 +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     
MED11 NM_001001683.2 -?/. - c.*6155C>T r.(=) p.(=)
ZMYND15 NM_001136046.2 -?/. - c.-739C>T r.(?) p.(=)
CXCL16 NM_022059.2 -?/. - c.55G>A r.(?) p.(Glu19Lys)


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