Variant #0000689161 (NC_000003.11:g.9739391C>T, MTMR14(NM_001077525.2):c.1614-4C>T)

Chromosome 3
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.9739391C>T
DNA change (hg38) -
Published as MTMR14(NM_022485.4):c.1434-4083C>T
ISCN -
DB-ID MTMR14_000041
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (large NGS studies) Variant not found in online data sets
Owner VKGL-NL_Groningen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTMR14 NM_001077525.2 -?/. - c.1614-4C>T r.spl? p.?