Variant #0001016576 (NC_000006.11:g.51944692A>G, NC_000006.11(NM_138694.3):c.390+6T>C (PKHD1))

Chromosome 6
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.51944692A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID PKHD1_000699
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-11-07 09:19:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PKHD1 NM_138694.3 +/. - c.390+6T>C r.(?) p.(?)


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