Variant #0000556695 (NC_000016.9:g.1568268G>A, NM_014714.3:c.4131C>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.1568268G>A
DNA change (hg38) g.1518267G>A
Published as IFT140(NM_014714.3):c.4131C>T (p.D1377=)
ISCN -
DB-ID IFT140_000125
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) 2.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-07 13:28:17 +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.4131C>T r.(?) p.(Asp1377=)
TELO2 NM_016111.3 -?/. - c.*8331G>A r.(=) p.(=)
TMEM204 NM_024600.5 -?/. - c.-16009G>A r.(?) p.(=)


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