Variant #0000548633 (NC_000012.11:g.54675155C>T, NC_000012.11(NM_031157.2):c.16-15C>T (HNRNPA1))

Chromosome 12
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.54675155C>T
DNA change (hg38) g.54281371C>T
Published as HNRNPA1(NM_031157.4):c.16-15C>T
ISCN -
DB-ID HNRNPA1_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) 0.00032 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 2019-07-18 18:22:55 +02:00 (CEST)
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     
CBX5 NM_012117.2 -?/. - c.-1406G>A r.(?) p.(=)
HNRNPA1 NM_031157.2 -?/. - c.16-15C>T r.(=) p.(=)


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