Variant #0000536818 (NC_000009.11:g.135936678A>G, NM_001807.4:c.-703A>G (CEL))

Chromosome 9
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.135936678A>G
DNA change (hg38) g.133061291A>G
Published as LOC100996574(XM_003846374.2):c.42T>C (p.(=))
ISCN -
DB-ID GTF3C5_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) Retrieve
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 2023-04-16 21:50:28 +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.*3311A>G r.(=) p.(=)
CEL NM_001807.4 -/. - c.-703A>G r.(?) p.(=)


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