Variant #0000866832 (NC_000022.10:g.37154436G>A, NM_006860.4:c.477C>T (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.37154436G>A
DNA change (hg38) -
Published as IFT27(NM_001177701.3):c.480C>T (p.F160=), IFT27(NM_006860.5):c.477C>T (p.F159=)
ISCN -
DB-ID IFT27_000015 See all 2 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) 0.00019 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 16:01:56 +02:00 (CEST)
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     
IFT27 NM_001177701.2 -?/. - c.480C>T r.(?) p.(Phe160=)
IFT27 NM_006860.4 -?/. - c.477C>T r.(?) p.(Phe159=)


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