Variant #0000277062 (NC_000019.9:g.14590236C>T, NM_005716.3:c.756G>A (GIPC1))

Chromosome 19
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.14590236C>T
DNA change (hg38) g.14479424C>T
Published as GIPC1(NM_005716.4):c.756G>A (p.T252=)
ISCN -
DB-ID GIPC1_000002 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) 0.32011 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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.-4180G>A - r.(?) p.(=)
GIPC1 NM_005716.3 -/. - c.756G>A - r.(?) p.(Thr252=)


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