Variant #0000247155 (NC_000012.11:g.57906143A>G, NC_000012.11(NM_004990.3):c.1753+7A>G (MARS))

Chromosome 12
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.57906143A>G
DNA change (hg38) g.57512360A>G
Published as MARS1(NM_004990.4):c.1753+7A>G
ISCN -
DB-ID MARS_000018
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) 0.00434 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDIT3 NM_004083.5 -/. - c.*4449T>C r.(=) p.(=)
MARS NM_004990.3 -/. - c.1753+7A>G r.(=) p.(=)


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