Variant #0000612070 (NC_000009.11:g.27062615G>T, NM_001031689.2:c.-115572C>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.27062615G>T
DNA change (hg38) g.27062617G>T
Published as IFT74(NM_001099222.3):c.1685-1G>T
ISCN -
DB-ID IFT74_000018 See all 4 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) 2.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLAA NM_001031689.2 ?/. - c.-115572C>A r.(?) p.(=)
LRRC19 NM_022901.2 ?/. - c.-57035C>A r.(?) p.(=)
IFT74 NM_025103.2 ?/. - c.1685-1G>T r.spl? p.?


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