Variant #0000965493 (NC_000009.11:g.72349198_72349201dup, NC_000009.11(NM_001099666.1):c.324-8_324-5dup (PTAR1))

Chromosome 9
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.72349198_72349201dup
DNA change (hg38) -
Published as PTAR1(NM_001099666.2):c.324-8_324-5dupTTTT
ISCN -
DB-ID PTAR1_000001
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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PTAR1 NM_001099666.1 -/. - c.324-8_324-5dup r.spl? p.?


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