Variant #0001027082 (NC_000017.10:g.8141897C>G, NM_025099.5:c.248G>C (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.8141897C>G
DNA change (hg38) -
Published as CTC1(NM_025099.5):c.248G>C (p.(Ser83Thr)), CTC1(NM_025099.6):c.248G>C (p.S83T)
ISCN -
DB-ID CTC1_000052 See all 4 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) 0.00885 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-02-07 18:57:27 +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     
CTC1 NM_025099.5 -?/. - c.248G>C r.(?) p.(Ser83Thr)


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