Variant #0000925030 (NC_000009.11:g.27029023_27029030del, NM_001031689.2:c.-81982_-81975del (PLAA))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.27029023_27029030del
DNA change (hg38) -
Published as IFT74(NM_025103.4):c.975-5_977delAACAGGTT
ISCN -
DB-ID IFT74_000037
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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.-81982_-81975del r.(?) p.(=)
LRRC19 NM_022901.2 +/. - c.-23445_-23438del r.(?) p.(=)
IFT74 NM_025103.2 +/. - c.975_982del r.(?) p.(Leu326Tyrfs*10)


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