Variant #0001068048 (NC_000008.10:g.110476498C>A, NM_177531.4:c.7437C>A (PKHD1L1))

Chromosome 8
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.110476498C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID PKHD1L1_000021 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs529097022
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00023 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-02 17:07:02 +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.7437C>A r.(?) p.(His2479Gln)


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