Variant #0000132572 (NC_000007.13:g.83689870T>C, NM_006080.2:c.458A>G (SEMA3A))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.83689870T>C
DNA change (hg38) g.84060554T>C
Published as -
ISCN -
DB-ID SEMA3A_000008 See all 5 reported entries
Variant remarks cDNA expression cloning in GN11 cells (embryonic) showed reduced SEMA3A signaling activity and in COS7 cells normal SEMA3A secretion
Reference PubMed: Hanchate 2012, Journal: Hanchate 2012
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00231 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-10-21 16:42:56 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEMA3A NM_006080.2 +/. 5 c.458A>G r.(?) p.Asn153Ser


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