Variant #0000323736 (NC_000014.8:g.68050491C>T, NM_004569.3:c.*6306G>A (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.68050491C>T
DNA change (hg38) g.67583774C>T
Published as PLEKHH1(NM_020715.2):c.3460C>T (p.(Pro1154Ser))
ISCN -
DB-ID PLEKHH1_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) 0.00273 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIGH NM_004569.3 ?/. - c.*6306G>A r.(=) p.(=)
PLEKHH1 NM_020715.2 ?/. - c.3460C>T r.(?) p.(Pro1154Ser)


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