Variant #0000261478 (NC_000010.10:g.97956579C>A, NC_000010.10(NM_013314.3):c.1251+85G>T (BLNK))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.97956579C>A
DNA change (hg38) g.96196823C>A
Published as BLNK(NM_013314.3):c.1251+85G>T
ISCN -
DB-ID BLNK_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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BLNK NM_013314.3 -/. - c.1251+85G>T r.(=) p.(=)
ZNF518A NM_014803.3 -/. - c.*36049C>A r.(=) p.(=)


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