Variant #0000283419 (NC_000007.13:g.26236235T>C, NM_002137.3:c.519A>G (HNRNPA2B1))

Chromosome 7
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.26236235T>C
DNA change (hg38) g.26196615T>C
Published as HNRNPA2B1(NM_031243.3):c.555A>G (p.R185=)
ISCN -
DB-ID HNRNPA2B1_000011
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) 0.01179 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
HNRNPA2B1 NM_002137.3 -?/. - c.519A>G r.(?) p.(Arg173=)
CBX3 NM_007276.4 -?/. - c.-4975T>C r.(?) p.(=)


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