Variant #0001036331 (NC_000007.13:g.26237238A>G, NC_000007.13(NM_002137.3):c.117+4T>C (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.26237238A>G
DNA change (hg38) -
Published as HNRNPA2B1(NM_002137.4):c.117+4T>C, HNRNPA2B1(NM_031243.2):c.153+4T>C, HNRNPA2B1(NM_031243.3):c.153+4T>C
ISCN -
DB-ID CBX3_000004 See all 3 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) 0.02875 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNRNPA2B1 NM_002137.3 -?/. - c.117+4T>C r.spl? p.?
CBX3 NM_007276.4 -?/. - c.-3972A>G r.(?) p.(=)


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