Variant #0000888685 (NC_000009.11:g.135940048T>C, NM_001807.4:c.248T>C (CEL))

Chromosome 9
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.135940048T>C
DNA change (hg38) -
Published as CEL(NM_001807.3):c.248T>C (p.(Phe83Ser)), CEL(NM_001807.4):c.248T>C (p.F83S)
ISCN -
DB-ID GTF3C5_000004 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) 0.00059 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 2022-11-01 13:01:21 +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     
GTF3C5 NM_001122823.1 -?/. - c.*6681T>C r.(=) p.(=)
CEL NM_001807.4 -?/. - c.248T>C r.(?) p.(Phe83Ser)


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