Variant #0001003884 (NC_000017.10:g.8139428T>C, NM_025099.5:c.1025A>G (CTC1))

Chromosome 17
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.8139428T>C
DNA change (hg38) -
Published as CTC1(NM_025099.5):c.1025A>G (p.(Asp342Gly)), CTC1(NM_025099.6):c.1025A>G (p.D342G)
ISCN -
DB-ID CTC1_000126 See all 2 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) 0.0032 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTC1 NM_025099.5 -?/. - c.1025A>G r.(?) p.(Asp342Gly)


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