Variant #0000279608 (NC_000012.11:g.57883193C>T, NC_000012.11(NM_004990.3):c.280-14C>T (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.57883193C>T
DNA change (hg38) g.57489410C>T
Published as MARS1(NM_004990.4):c.280-14C>T
ISCN -
DB-ID MARS_000015 See all 2 reported entries
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) 0.00278 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.*27399G>A r.(=) p.(=)
MARS NM_004990.3 -/. - c.280-14C>T r.(=) p.(=)
GLI1 NM_005269.2 -/. - c.*17349C>T r.(=) p.(=)
ARHGAP9 NM_032496.2 -/. - c.-9699G>A r.(?) p.(=)


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