Variant #0000408545 (NC_000014.8:g.23790713G>C, NM_004643.3:c.35G>C (PABPN1))

Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.23790713G>C
DNA change (hg38) g.23321504G>C
Published as Ala[13]
ISCN -
DB-ID PABPN1_000017 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2011-01-16 11:38:09 +01:00 (CET)
Date last edited 2012-11-02 20:42:58 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
PABPN1 NM_004643.3 ?/. 1 c.35G>C - r.(?) p.(Gly12Ala)


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