Variant #0000617128 (NC_000018.9:g.32707060_32707062dup, NC_000018.9(NM_014268.3):c.750+9_750+11dup (MAPRE2))

Chromosome 18
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.32707060_32707062dup
DNA change (hg38) g.35127096_35127098dup
Published as MAPRE2(NM_001143826.2):c.621+6_621+7insCAT (p.(=))
ISCN -
DB-ID MAPRE2_000007
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAPRE2 NM_014268.3 -?/. - c.750+9_750+11dup r.(=) p.(=)


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