Variant #0000614934 (NC_000014.8:g.24040444dup, NM_003917.2:c.-3494dup (AP1G2))

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.24040444dup
DNA change (hg38) g.23571235dup
Published as JPH4(NM_032452.2):c.1504dupG (p.A502Gfs*12)
ISCN -
DB-ID AP1G2_000009
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-05 13:36:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
THTPA NM_001126339.2 ?/. - c.*12395dup r.(?) p.(=)
AP1G2 NM_003917.2 ?/. - c.-3494dup r.(?) p.(=)
JPH4 NM_032452.2 ?/. - c.1504dup r.(?) p.(Ala502GlyfsTer12)


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