Variant #0001072300 (NC_000008.10:g.110492352C>T, NM_177531.4:c.9311C>T (PKHD1L1))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.110492352C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID PKHD1L1_000047
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs117952538
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.01082 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-10 12:06:02 +02:00 (CEST)
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.9311C>T r.(?) p.(Thr3104Ile)


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