Variant #0000265086 (NC_000016.9:g.30910830C>T, NM_001330.3:c.120C>T (CTF1))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.30910830C>T
DNA change (hg38) g.30899509C>T
Published as CTF1(NM_001330.5):c.120C>T (p.Y40=)
ISCN -
DB-ID CTF1_000001
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) 0.00549 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTF1 NM_001330.3 -/. - c.120C>T r.(?) p.(Tyr40=)
BCL7C NM_004765.2 -/. - c.-5565G>A r.(?) p.(=)


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