Variant #0000676813 (NC_000003.11:g.129207102C>T, NM_052985.2:c.2007C>T (IFT122))

Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.129207102C>T
DNA change (hg38) -
Published as IFT122(NM_001280541.1):c.1830C>T (p.(=)), IFT122(NM_052985.3):c.2007C>T (p.S669=), IFT122(NM_052985.4):c.2007C>T (p.S669=)
ISCN -
DB-ID IFT122_000046 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) 0.00253 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFT122 NM_052985.2 -/. - c.2007C>T r.(?) p.(Ser669=)


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