Variant #0001021202 (NC_000022.10:g.31333938_31333946dup, NM_001303256.2:c.1235_1243dup (MORC2))

Chromosome 22
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.31333938_31333946dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID MORC2_000070
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1555938722
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-01-21 10:35:01 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MORC2 NM_001303256.2 ?/. - c.1235_1243dup r.(?) p.(Gly412_Val414dup)


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