Variant #0000531102 (NC_000007.13:g.143965476C>T, NM_001005328.1:c.-8755G>A (OR2A7))

Chromosome 7
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.143965476C>T
DNA change (hg38) g.144268383C>T
Published as CTAGE8(NM_001278507.1):c.868G>A (p.D290N)
ISCN -
DB-ID OR2A7_000003
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 2019-07-18 18:22:55 +02:00 (CEST)
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     
OR2A7 NM_001005328.1 -/. - c.-8755G>A r.(?) p.(=)
CTAGE8 NM_001278507.1 -/. - c.868G>A r.(?) p.(Asp290Asn)
ARHGEF34P NR_033942.1 -/. - n.3567+4062G>A r.(?) -


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