Variant #0000866833 (NC_000022.10:g.37160049T>C, NM_006860.4:c.263A>G (IFT27))

Chromosome 22
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.37160049T>C
DNA change (hg38) -
Published as IFT27(NM_001177701.2):c.266A>G (p.Y89C)
ISCN -
DB-ID IFT27_000016
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFT27 NM_001177701.2 ?/. - c.266A>G r.(?) p.(Tyr89Cys)
IFT27 NM_006860.4 ?/. - c.263A>G r.(?) p.(Tyr88Cys)


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