Variant #0001055320 (NC_000016.9:g.1556969G>C, NM_014714.3:c.*3976C>G (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.1556969G>C
DNA change (hg38) -
Published as TELO2(NM_016111.4):c.2143G>C (p.(Asp715His))
ISCN -
DB-ID IFT140_000344
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IFT140 NM_014714.3 ?/. - c.*3976C>G r.(=) p.(=)
TELO2 NM_016111.3 ?/. - c.2143G>C r.(?) p.(Asp715His)
TMEM204 NM_024600.5 ?/. - c.-27308G>C r.(?) p.(=)


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