Variant #0000304818 (NC_000001.10:g.248813457_248813458del, NM_001001824.1:c.732_733del (OR2T27))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.248813457_248813458del
DNA change (hg38) g.248650156_248650157del
Published as OR2T27(NM_001001824.1):c.732_733delCA (p.M245Gfs*24)
ISCN -
DB-ID OR2T27_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_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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OR2T27 NM_001001824.1 ?/. - c.732_733del r.(?) p.(Met245GlyfsTer24)


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