Variant #0000980397 (NC_000012.11:g.57884125G>A, NM_004990.3:c.626G>A (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.57884125G>A
DNA change (hg38) -
Published as MARS(NM_004990.4):c.626G>A (p.(Ser209Asn)), MARS1(NM_004990.4):c.626G>A (p.S209N)
ISCN -
DB-ID ARHGAP9_000004 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) 0.00085 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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.*26467C>T r.(=) p.(=)
MARS NM_004990.3 -?/. - c.626G>A r.(?) p.(Ser209Asn)
GLI1 NM_005269.2 -?/. - c.*18281G>A r.(=) p.(=)
ARHGAP9 NM_032496.2 -?/. - c.-10631C>T r.(?) p.(=)


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