Variant #0000000735 (NC_000007.14:g.116699618C>T, NM_001127500.2:c.534C>T (MET))

Individual ID 00000143
Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.116699618C>T
Published as 116339672C>T
Reference Nurul-Syakima Ab Mutalib et al. (2014)dbSNP
DB-ID MET_000001
dbSNP ID rs35775721
Frequency 1/9
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2020-11-09 10:01:07 +08:00 (CST)
Date last edited 2021-08-23 08:59:14 +08:00 (CST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
MET NM_001127500.2 -/. - c.534C>T - r.(=) p.(=) - ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000158 DNA SEQ-NG;PCR MET 1 Nuur Athirah Binti Mohd Daud