Variant #0000515563 (NC_000002.11:g.27668307_27668310del, NM_015662.1:c.4925_4928del (IFT172))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.27668307_27668310del
DNA change (hg38) g.27445440_27445443del
Published as IFT172(NM_015662.3):c.4925_4928delGAGA (p.R1642Kfs*32)
ISCN -
DB-ID IFT172_000073 See all 3 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +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     
NRBP1 NM_013392.2 +/. - c.*3628_*3631del r.(=) p.(=)
IFT172 NM_015662.1 +/. - c.4925_4928del r.(?) p.(Arg1642LysfsTer32)
KRTCAP3 NM_173853.3 +/. - c.*1260_*1263del r.(=) p.(=)


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