Variant #0001065056 (NC_000009.11:g.26961982A>C, NM_001031689.2:c.-14939T>G (PLAA))

Chromosome 9
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.26961982A>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID IFT74_000045
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLAA NM_001031689.2 ?/. - c.-14939T>G r.(?) p.(=)
LRRC19 NM_022901.2 ?/. - c.*33537T>G r.(=) p.(=)
IFT74 NM_025103.2 ?/. - c.17A>C r.(?) p.(Lys6Thr)


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