Variant #0000860397 (NC_000006.11:g.51747977A>C, NM_138694.3:c.7264T>G (PKHD1))

Chromosome 6
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.51747977A>C
DNA change (hg38) -
Published as PKHD1(NM_138694.3):c.7264T>G (p.(Cys2422Gly)), PKHD1(NM_138694.4):c.7264T>G (p.C2422G)
ISCN -
DB-ID PKHD1_000092 See all 4 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) 0.00053 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PKHD1 NM_138694.3 ?/. - c.7264T>G r.(?) p.(Cys2422Gly)


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