Variant #0000913916 (NC_000012.11:g.57884356T>G, NM_004990.3:c.699T>G (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.57884356T>G
DNA change (hg38) -
Published as MARS1(NM_004990.4):c.699T>G (p.I233M)
ISCN -
DB-ID ARHGAP9_000013
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) 0.00012 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 2023-01-11 15:44:22 +01:00 (CET)
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.*26236A>C r.(=) p.(=)
MARS NM_004990.3 ?/. - c.699T>G r.(?) p.(Ile233Met)
GLI1 NM_005269.2 ?/. - c.*18512T>G r.(=) p.(=)
ARHGAP9 NM_032496.2 ?/. - c.-10862A>C r.(?) p.(=)


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