Variant #0000536823 (NC_000009.11:g.135940439T>G, NM_001807.4:c.362T>G (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.135940439T>G
DNA change (hg38) g.133065052T>G
Published as CEL(NM_001807.3):c.362T>G (p.(Leu121Arg))
ISCN -
DB-ID GTF3C5_000006
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) 0.00435 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.*7072T>G r.(=) p.(=)
CEL NM_001807.4 -?/. - c.362T>G r.(?) p.(Leu121Arg)


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