Variant #0000914468 (NC_000016.9:g.1561037G>A, NM_014714.3:c.4297C>T (IFT140))

Chromosome 16
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.1561037G>A
DNA change (hg38) -
Published as IFT140(NM_014714.3):c.4297C>T (p.R1433C, p.(Arg1433Cys)), IFT140(NM_014714.4):c.4297C>T (p.R1433C)
ISCN -
DB-ID IFT140_000062 See all 6 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) 0.00083 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFT140 NM_014714.3 -?/. - c.4297C>T r.(?) p.(Arg1433Cys)
TELO2 NM_016111.3 -?/. - c.*1100G>A r.(=) p.(=)
TMEM204 NM_024600.5 -?/. - c.-23240G>A r.(?) p.(=)


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