Variant #0000305895 (NC_000014.8:g.68053899C>T, NM_004569.3:c.*2898G>A (PIGH))

Chromosome 14
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.68053899C>T
DNA change (hg38) g.67587182C>T
Published as PLEKHH1(NM_020715.2):c.4042C>T (p.R1348*)
ISCN -
DB-ID PIGH_000001 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) 0.00766 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 2020-07-05 15:17:04 +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.*2898G>A r.(=) p.(=)
PLEKHH1 NM_020715.2 -/. - c.4042C>T r.(?) p.(Arg1348Ter)


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