Variant #0000944619 (NC_000008.10:g.110418707G>A, NM_177531.4:c.1813G>A (PKHD1L1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.110418707G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID PKHD1L1_000017
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs767753360
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 5.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-11-10 08:00:01 +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     
PKHD1L1 NM_177531.4 +?/. - c.1813G>A r.(?) p.(Gly605Arg)


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