Variant #0000890703 (NC_000012.11:g.57883674del, NC_000012.11(NM_004990.3):c.415-5del (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.57883674del
DNA change (hg38) -
Published as MARS1(NM_004990.4):c.415-5delC
ISCN -
DB-ID ARHGAP9_000012
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) 6.0E-5 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 2022-11-01 13:01:21 +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.*26918del r.(?) p.(=)
MARS NM_004990.3 -?/. - c.415-5del r.spl? p.?
GLI1 NM_005269.2 -?/. - c.*17830del r.(?) p.(=)
ARHGAP9 NM_032496.2 -?/. - c.-10180del r.(?) p.(=)


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