Variant #0000930121 (NC_000012.11:g.57908633C>T, NM_004990.3:c.2098C>T (MARS))

Chromosome 12
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.57908633C>T
DNA change (hg38) -
Published as MARS1(NM_004990.4):c.2098C>T (p.R700W)
ISCN -
DB-ID DDIT3_000026
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) 2.0E-5 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 2023-07-07 10:10:56 +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     
DDIT3 NM_004083.5 ?/. - c.*1959G>A r.(=) p.(=)
MARS NM_004990.3 ?/. - c.2098C>T r.(?) p.(Arg700Trp)


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