Variant #0000536819 (NC_000009.11:g.135937396C>T, NM_001807.4:c.16C>T (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.135937396C>T
DNA change (hg38) g.133062009C>T
Published as CEL(NM_001807.3):c.16C>T (p.(Arg6Cys))
ISCN -
DB-ID GTF3C5_000002
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) 0.00246 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GTF3C5 NM_001122823.1 -?/. - c.*4029C>T r.(=) p.(=)
CEL NM_001807.4 -?/. - c.16C>T r.(?) p.(Arg6Cys)


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