Variant #0000273087 (NC_000009.11:g.135946015T>C, NM_001807.4:c.1463T>C (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.135946015T>C
DNA change (hg38) g.133070628T>C
Published as CEL(NM_001807.3):c.1463T>C (p.(Ile488Thr)), CEL(NM_001807.4):c.1463T>C (p.I488T)
ISCN -
DB-ID CEL_000001 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
CEL NM_001807.4 -/. - c.1463T>C r.(?) p.(Ile488Thr)


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