Variant #0000615805 (NC_000016.9:g.1642227A>G, NM_014714.3:c.584T>C (IFT140))

Chromosome 16
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.1642227A>G
DNA change (hg38) g.1592226A>G
Published as IFT140(NM_014714.3):c.584T>C (p.L195P), IFT140(NM_014714.4):c.584T>C (p.(Leu195Pro))
ISCN -
DB-ID IFT140_000176 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 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFT140 NM_014714.3 ?/. - c.584T>C r.(?) p.(Leu195Pro)
TELO2 NM_016111.3 ?/. - c.*82290A>G r.(=) p.(=)
TMEM204 NM_024600.5 ?/. - c.*37200A>G r.(=) p.(=)


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