Variant #0000291512 (NC_000002.11:g.198571707_198571725del, NM_138395.3:c.1578_1596del (MARS2))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.198571707_198571725del
DNA change (hg38) g.197706983_197707001del
Published as MARS2(NM_138395.3):c.1578_1596delTGTCACCCCAAGCCTAGCT (p.V527Tfs*48)
ISCN -
DB-ID MARS2_000006
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MARS2 NM_138395.3 +/. - c.1578_1596del r.(?) p.(Val527ThrfsTer48)


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