Variant #0000562105 (NC_000017.10:g.4647966G>A, NM_022059.2:c.-5275C>T (CXCL16))

Chromosome 17
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.4647966G>A
DNA change (hg38) g.4744671G>A
Published as ZMYND15(NM_001136046.3):c.1730G>A (p.R577Q), ZMYND15(NM_001267822.1):c.1730G>A (p.R577Q)
ISCN -
DB-ID CXCL16_000001 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) 0.00015 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MED11 NM_001001683.2 ?/. - c.*11484G>A r.(=) p.(=)
ZMYND15 NM_001136046.2 ?/. - c.1730G>A r.(?) p.(Arg577Gln)
CXCL16 NM_022059.2 ?/. - c.-5275C>T r.(?) p.(=)


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