Variant #0000546478 (NC_000012.11:g.110605665_110605669del, NC_000012.11(NM_014055.3):c.1188+4795_1188+4799del (IFT81))

Chromosome 12
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.110605665_110605669del
DNA change (hg38) g.110167860_110167864del
Published as IFT81(NM_014055.4):c.1188+4795_1188+4799delTTTTT
ISCN -
DB-ID IFT81_000005
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
IFT81 NM_014055.3 -/. - c.1188+4795_1188+4799del r.(=) p.(=)


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