Variant #0000614319 (NC_000012.11:g.57905559C>T, NM_004990.3:c.1447C>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.57905559C>T
DNA change (hg38) g.57511776C>T
Published as MARS1(NM_004990.4):c.1447C>T (p.R483C)
ISCN -
DB-ID DDIT3_000011
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) 0.00018 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DDIT3 NM_004083.5 ?/. - c.*5033G>A r.(=) p.(=)
MARS NM_004990.3 ?/. - c.1447C>T r.(?) p.(Arg483Cys)


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