Variant #0000323795 (NC_000014.8:g.89307227A>G, NM_144596.2:c.284A>G (TTC8))

Chromosome 14
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.89307227A>G
DNA change (hg38) g.88840883A>G
Published as TTC8(NM_001288781.1):c.254A>G (p.K85R, p.(Lys85Arg)), TTC8(NM_144596.3):c.284A>G (p.K95R)
ISCN -
DB-ID TTC8_000045 See all 10 reported entries
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) 0.00543 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTC8 NM_144596.2 -?/. - c.284A>G r.(?) p.(Lys95Arg)


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