Variant #0000046845 (NC_000014.8:g.89338702A>G, NM_144596.2:c.1253A>G (TTC8))

Chromosome 14
Allele Both (homozygous)
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.89338702A>G
DNA change (hg38) g.88872358A>G
Published as -
ISCN -
DB-ID TTC8_000029 See all 8 reported entries
Variant remarks -
Reference Journal: Lim et al. (2014)
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation yes
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00296 View details
Owner Marianne Vos (LOVD-team)
Database submission license No license selected
Created by Marianne Vos (LOVD-team)
Date created 2014-11-13 12:07:54 +01:00 (CET)
Date last edited 2016-03-11 11:30:15 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTC8 NM_144596.2 +?/. 13 c.1253A>G r.(?) p.(Gln418Arg)


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