Variant #0000548636 (NC_000012.11:g.54676175dup, NC_000012.11(NM_031157.2):c.491-3dup (HNRNPA1))

Chromosome 12
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.54676175dup
DNA change (hg38) g.54282391dup
Published as HNRNPA1(NM_031157.4):c.491-3dupT
ISCN -
DB-ID HNRNPA1_000012 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) Retrieve
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.-2417dup r.(?) p.(=)
HNRNPA1 NM_031157.2 -/. - c.491-3dup r.spl? p.?


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