Variant #0000280043 (NC_000011.9:g.95615695_95615699del, NC_000011.9(NM_016156.5):c.186+5654_186+5658del (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.95615695_95615699del
DNA change (hg38) g.95882531_95882535del
Published as MTMR2(NM_001243571.2):c.-153-6_-153-2delTTTTA
ISCN -
DB-ID MTMR2_000042
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 2018-01-15 20:58:59 +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     
MTMR2 NM_016156.5 -?/. - c.186+5654_186+5658del r.(=) p.(=)


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