Variant #0000858855 (NC_000003.11:g.160075272T>C, NC_000003.11(NM_020800.2):c.639+5A>G (IFT80))

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.160075272T>C
DNA change (hg38) -
Published as IFT80(NM_001190241.1):c.228+5A>G (p.?)
ISCN -
DB-ID IFT80_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) 0.00035 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +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     
SMC4 NM_001002800.1 -?/. - c.-42271T>C r.(?) p.(=)
IFT80 NM_020800.2 -?/. - c.639+5A>G r.spl? p.?


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