Variant #0000890702 (NC_000012.11:g.57881951A>G, NM_004990.3:c.78A>G (MARS))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.57881951A>G
DNA change (hg38) -
Published as MARS(NM_004990.3):c.78A>G (p.A26=), MARS1(NM_004990.4):c.78A>G (p.A26=)
ISCN -
DB-ID ARHGAP9_000007 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 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 2022-11-01 13:01:21 +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.*28641T>C r.(=) p.(=)
MARS NM_004990.3 -?/. - c.78A>G r.(?) p.(Ala26=)
GLI1 NM_005269.2 -?/. - c.*16107A>G r.(=) p.(=)
ARHGAP9 NM_032496.2 -?/. - c.-8457T>C r.(?) p.(=)


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