Variant #0000556987 (NC_000016.9:g.1639619_1639621del, NM_014714.3:c.800_802del (IFT140))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.1639619_1639621del
DNA change (hg38) g.1589618_1589620del
Published as IFT140(NM_014714.3):c.800_802delAAG (p.E267del)
ISCN -
DB-ID IFT140_000154
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_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 2020-03-23 16:13:27 +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.800_802del r.(?) p.(Glu267del)
TELO2 NM_016111.3 +?/. - c.*79682_*79684del r.(=) p.(=)
TMEM204 NM_024600.5 +?/. - c.*34592_*34594del r.(=) p.(=)


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