Variant #0000321706 (NC_000010.10:g.97916283C>A, NM_013314.3:c.*35446G>T (BLNK))

Chromosome 10
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.97916283C>A
DNA change (hg38) g.96156526C>A
Published as ZNF518A(NM_014803.3):c.204C>A (p.(Asp68Glu))
ISCN -
DB-ID ZNF518A_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) 0.00017 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 2020-06-29 09:39:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BLNK NM_013314.3 ?/. - c.*35446G>T r.(=) p.(=)
ZNF518A NM_014803.3 ?/. - c.204C>A r.(?) p.(Asp68Glu)


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