Variant #0000277860 (NC_000016.9:g.1574590C>T, NM_014714.3:c.3104G>A (IFT140))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1574590C>T
DNA change (hg38) g.1524589C>T
Published as IFT140(NM_014714.3):c.3104G>A (p.R1035Q, p.(Arg1035Gln)), IFT140(NM_014714.4):c.3104G>A (p.R1035Q)
ISCN -
DB-ID IFT140_000025 See all 5 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) 8.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +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.3104G>A r.(?) p.(Arg1035Gln)
TELO2 NM_016111.3 -/. - c.*14653C>T r.(=) p.(=)
TMEM204 NM_024600.5 -/. - c.-9687C>T r.(?) p.(=)


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