Variant #0000607894 (NC_000002.11:g.27716959dup, NM_015662.1:c.-4439dup (IFT172))

Chromosome 2
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.27716959dup
DNA change (hg38) g.27494092dup
Published as FNDC4(NM_022823.3):c.292dupA (p.T98Nfs*13)
ISCN -
DB-ID FNDC4_000001
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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GCKR NM_001486.3 ?/. - c.-2813dup r.(?) p.(=)
IFT172 NM_015662.1 ?/. - c.-4439dup r.(?) p.(=)
FNDC4 NM_022823.2 ?/. - c.292dup r.(?) p.(Thr98AsnfsTer13)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.