Variant #0000147271 (NC_000012.11:g.57908817G>A, NM_004990.3:c.2180G>A (MARS))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.57908817G>A
DNA change (hg38) g.57515034G>A
Published as -
ISCN -
DB-ID MARS_000013 See all 3 reported entries
Variant remarks expression cloning (orthologous yeast MES1 protein) able to rescue growth defect MES1 null allele
Reference PubMed: Gonzalez 2013
ClinVar ID -
dbSNP ID rs113808165
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0049 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 2016-12-02 11:52:55 +01:00 (CET)
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     
MARS NM_004990.3 -?/. 17 c.2180G>A r.(?) p.(Arg727Gln)


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