Variant #0000975648 (NC_000003.11:g.160073923C>T, NM_020800.2:c.655G>A (IFT80))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.160073923C>T
DNA change (hg38) -
Published as IFT80(NM_020800.3):c.655G>A (p.(Gly219Ser))
ISCN -
DB-ID IFT80_000049
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) 9.0E-5 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 2024-04-19 20:27:30 +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     
SMC4 NM_001002800.1 ?/. - c.-43620C>T r.(?) p.(=)
IFT80 NM_020800.2 ?/. - c.655G>A r.(?) p.(Gly219Ser)


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