Variant #0000518397 (NC_000003.11:g.160025451G>A, NM_020800.2:c.1076C>T (IFT80))

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.160025451G>A
DNA change (hg38) g.160307663G>A
Published as IFT80(NM_001190241.1):c.665C>T (p.(Ser222Phe)), IFT80(NM_020800.2):c.1076C>T (p.S359F)
ISCN -
DB-ID IFT80_000008 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) 0.01083 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SMC4 NM_001002800.1 -/. - c.-92092G>A r.(?) p.(=)
IFT80 NM_020800.2 -/. - c.1076C>T r.(?) p.(Ser359Phe)


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