Variant #0000331224 (NC_000006.11:g.132859712_132859714del, NM_175057.3:c.284_286del (TAAR9))

Chromosome 6
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.132859712_132859714del
DNA change (hg38) g.132538573_132538575del
Published as TAAR9(NM_175057.3):c.284_286del (p.(Glu95_Ser96delinsGly))
ISCN -
DB-ID TAAR9_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) 0.00118 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-22 10:24:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TAAR9 NM_175057.3 ?/. - c.284_286del r.(?) p.(Glu95_Ser96delinsGly)


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