Variant #0000442686 (NC_000003.11:g.9726968del, MTMR14(NM_001077525.2):c.1164+37del)

Individual ID 00210154
Chromosome 3
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.9726968del
DNA change (hg38) g.9685284del
Published as 1164+36delG
ISCN -
DB-ID MTMR14_000033
Variant remarks -
Reference PubMed: Tosch 2006
ClinVar ID -
dbSNP ID rs373359960
Origin Germline
Segregation -
Frequency 0.02
Re-site -
VIP 0
Methylation -
Average frequency (large NGS studies) 8.0E-5 View details
Owner Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTMR14 NM_001077525.2 -/- 13i c.1164+37del r.(=?) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000211230 DNA SEQ - - MTMR14 1 Johan den Dunnen