Variant #0000548769 (NC_000012.11:g.57881916G>C, NM_004990.3:c.43G>C (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.57881916G>C
DNA change (hg38) g.57488133G>C
Published as MARS1(NM_004990.4):c.43G>C (p.V15L)
ISCN -
DB-ID ARHGAP9_000002
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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.*28676C>G r.(=) p.(=)
MARS NM_004990.3 ?/. - c.43G>C r.(?) p.(Val15Leu)
GLI1 NM_005269.2 ?/. - c.*16072G>C r.(=) p.(=)
ARHGAP9 NM_032496.2 ?/. - c.-8422C>G r.(?) p.(=)


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