Variant #0000517819 (NC_000003.11:g.129196984C>T, NM_052985.2:c.1426C>T (IFT122))

Chromosome 3
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.129196984C>T
DNA change (hg38) g.129478141C>T
Published as IFT122(NM_001280541.1):c.1249C>T (p.(Arg417Trp)), IFT122(NM_052985.3):c.1426C>T (p.R476W), IFT122(NM_052985.4):c.1426C>T (p.R476W)
ISCN -
DB-ID IFT122_000020 See all 4 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) 0.00511 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFT122 NM_052985.2 -?/. - c.1426C>T r.(?) p.(Arg476Trp)


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