Variant #0000996262 (NC_000007.13:g.143956465T>A, NM_001005328.1:c.257A>T (OR2A7))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.143956465T>A
DNA change (hg38) -
Published as OR2A7(NM_001005328.1):c.257A>T (p.(His86Leu))
ISCN -
DB-ID OR2A7_000006
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OR2A7 NM_001005328.1 -?/. - c.257A>T r.(?) p.(His86Leu)
CTAGE8 NM_001278507.1 -?/. - c.*7545A>T r.(=) p.(=)
ARHGEF34P NR_033942.1 -?/. - n.3828A>T r.(?) -


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