Variant #0000949263 (NC_000009.11:g.27055671A>C, NM_001031689.2:c.-108628T>G (PLAA))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27055671A>C
DNA change (hg38) -
Published as IFT74(NM_001349928.2):c.1398A>C (p.E466D)
ISCN -
DB-ID IFT74_000039
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) 0.00048 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-11-27 17:35:39 +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.-108628T>G r.(?) p.(=)
LRRC19 NM_022901.2 -?/. - c.-50091T>G r.(?) p.(=)
IFT74 NM_025103.2 -?/. - c.1398A>C r.(?) p.(Glu466Asp)


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