Variant #0000215362 (NC_000002.11:g.27668310C>T, NM_015662.1:c.4921G>A (IFT172))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.27668310C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KRTCAP3_000078
Frequency 1/13004
Freq. EA 0/8598
Freq. AA 1/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:22:05 +02:00 (CEST)
Date last edited 2013-05-03 21:57:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
IFT172 NM_015662.1 ?/? c.4921G>A r.(?) p.(Glu1641Lys)
KRTCAP3 NM_173853.3 ?/? c.*1263C>T r.(?) p.(Glu1641Lys)