Variant #0000888795 (NC_000009.11:g.26984358G>A, NM_001031689.2:c.-37315C>T (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.26984358G>A
DNA change (hg38) -
Published as IFT74(NM_001099222.1):c.404+5G>A (p.?), IFT74(NM_001349928.2):c.404+5G>A
ISCN -
DB-ID IFT74_000030 See all 2 reported entries
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:01:21 +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     
PLAA NM_001031689.2 ?/. - c.-37315C>T r.(?) p.(=)
LRRC19 NM_022901.2 ?/. - c.*11161C>T r.(=) p.(=)
IFT74 NM_025103.2 ?/. - c.404+5G>A r.spl? p.?


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