Variant #0000546146 (NC_000011.9:g.95583916_95583917insTACTCTAAAAGAGGGT, NC_000011.9(NM_016156.5):c.655-4_655-3insACCCTCTTTTAGAGTA (MTMR2))

Chromosome 11
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.95583916_95583917insTACTCTAAAAGAGGGT
DNA change (hg38) g.95850752_95850753insTACTCTAAAAGAGGGT
Published as MTMR2(NM_001243571.2):c.439-4_439-3insACCCTCTTTTAGAGTA
ISCN -
DB-ID MTMR2_000052
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-01 11:16:14 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTMR2 NM_016156.5 -?/. - c.655-4_655-3insACCCTCTTTTAGAGTA r.spl? p.?


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.