Variant #0000800965 (NC_000003.11:g.129195600G>A, NM_052985.2:c.1256G>A (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.129195600G>A
DNA change (hg38) -
Published as IFT122(NM_001280541.1):c.1079G>A (p.(Ser360Asn)), IFT122(NM_052985.3):c.1256G>A (p.S419N)
ISCN -
DB-ID IFT122_000018 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) 0.0029 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFT122 NM_052985.2 -?/. - c.1256G>A r.(?) p.(Ser419Asn)


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