Variant #0000556989 (NC_000016.9:g.1642461C>T, NC_000016.9(NM_014714.3):c.491+7G>A (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.1642461C>T
DNA change (hg38) g.1592460C>T
Published as IFT140(NM_014714.4):c.491+7G>A
ISCN -
DB-ID IFT140_000156
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) 0.00059 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFT140 NM_014714.3 -?/. - c.491+7G>A r.(=) p.(=)
TELO2 NM_016111.3 -?/. - c.*82524C>T r.(=) p.(=)
TMEM204 NM_024600.5 -?/. - c.*37434C>T r.(=) p.(=)


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