Variant #0000571914 (NC_000022.10:g.37154368C>T, NM_006860.4:c.545G>A (IFT27))

Chromosome 22
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.37154368C>T
DNA change (hg38) g.36758324C>T
Published as IFT27(NM_001177701.2):c.548G>A (p.R183Q)
ISCN -
DB-ID IFT27_000007
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) 8.0E-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 2019-07-18 18:22:55 +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.548G>A r.(?) p.(Arg183Gln)
IFT27 NM_006860.4 -?/. - c.545G>A r.(?) p.(Arg182Gln)


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