Variant #0001054930 (NC_000014.8:g.89307769G>A, NM_144596.2:c.490G>A (TTC8))

Chromosome 14
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.89307769G>A
DNA change (hg38) -
Published as TTC8(NM_001288781.1):c.460G>A (p.A154T), TTC8(NM_144596.3):c.490G>A (p.A164T), TTC8(NM_144596.4):c.490G>A (p.(Ala164Thr))
ISCN -
DB-ID TTC8_000057 See all 3 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) 1.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTC8 NM_144596.2 ?/. - c.490G>A r.(?) p.(Ala164Thr)


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