Variant #0001066330 (NC_000016.9:g.1570590G>A, NC_000016.9(NM_014714.3):c.3660+13C>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.1570590G>A
DNA change (hg38) -
Published as IFT140(NM_014714.3):c.3660+13C>T (p.(=))
ISCN -
DB-ID IFT140_000350
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) 6.0E-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 2026-01-20 18:57:21 +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.3660+13C>T r.(=) p.(=)
TELO2 NM_016111.3 -?/. - c.*10653G>A r.(=) p.(=)
TMEM204 NM_024600.5 -?/. - c.-13687G>A r.(?) p.(=)


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