Variant #0000289146 (NC_000007.13:g.26233189T>C, NC_000007.13(NM_002137.3):c.841+6A>G (HNRNPA2B1))

Chromosome 7
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.26233189T>C
DNA change (hg38) g.26193569T>C
Published as HNRNPA2B1(NM_031243.2):c.877+6A>G, HNRNPA2B1(NM_031243.3):c.877+6A>G
ISCN -
DB-ID HNRNPA2B1_000004 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) 0.00162 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 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.841+6A>G r.(=) p.(=)


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