Variant #0000612834 (NC_000010.10:g.97951797C>T, NM_013314.3:c.1303G>A (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.97951797C>T
DNA change (hg38) g.96192041C>T
Published as BLNK(NM_013314.4):c.1303G>A (p.V435I)
ISCN -
DB-ID BLNK_000010
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BLNK NM_013314.3 ?/. - c.1303G>A r.(?) p.(Val435Ile)
ZNF518A NM_014803.3 ?/. - c.*31267C>T r.(=) p.(=)


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