Variant #0000852238 (NC_000009.11:g.27062709C>T, NM_001031689.2:c.-115666G>A (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.27062709C>T
DNA change (hg38) -
Published as IFT74(NM_025103.3):c.1778C>T (p.A593V)
ISCN -
DB-ID IFT74_000034
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:40:45 +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     
PLAA NM_001031689.2 ?/. - c.-115666G>A r.(?) p.(=)
LRRC19 NM_022901.2 ?/. - c.-57129G>A r.(?) p.(=)
IFT74 NM_025103.2 ?/. - c.1778C>T r.(?) p.(Ala593Val)


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