Variant #0000306599 (NC_000019.9:g.14584811C>G, NM_005716.3:c.*4417G>C (GIPC1))

Chromosome 19
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.14584811C>G
DNA change (hg38) g.14473999C>G
Published as PTGER1(NM_000955.3):c.322G>C (p.G108R)
ISCN -
DB-ID PTGER1_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) 5.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
PTGER1 NM_000955.2 ?/. - c.322G>C - r.(?) p.(Gly108Arg)
PKN1 NM_002741.3 ?/. - c.*2215C>G - r.(=) p.(=)
GIPC1 NM_005716.3 ?/. - c.*4417G>C - r.(=) p.(=)


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