Variant #0000691694 (NC_000014.8:g.68056880G>C, NM_004569.3:c.484C>G (PIGH))

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.68056880G>C
DNA change (hg38) -
Published as PIGH(NM_004569.5):c.484C>G (p.P162A)
ISCN -
DB-ID PIGH_000006
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIGH NM_004569.3 ?/. - c.484C>G r.(?) p.(Pro162Ala)
PLEKHH1 NM_020715.2 ?/. - c.*2928G>C r.(=) p.(=)


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