Variant #0000915262 (NC_000019.9:g.4817911G>A, NM_182919.3:c.479C>T (TICAM1))

Chromosome 19
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.4817911G>A
DNA change (hg38) -
Published as TICAM1(NM_182919.3):c.479C>T (p.S160F), TICAM1(NM_182919.4):c.479C>T (p.S160F)
ISCN -
DB-ID TICAM1_000029 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) 0.00219 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TICAM1 NM_182919.3 -?/. - c.479C>T r.(?) p.(Ser160Phe)


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