Variant #0000007301 (NC_000007.14:g.116795714C>T, MET(NM_001127500.2):c.3912C>T)

Individual ID 00001283
Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Does not affect function
DNA change (genomic) (Relative to hg38 / GRCh38) g.116795714C>T
Reference -
DB-ID MET_000002 See all 4 reported entries
dbSNP ID -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Silvina Sisterna-Hospital de Comunidad
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Instituto Nacional del Cancer
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Protein     

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Co_ocurrence     

RNA change     

Review status     
MET NM_001127500.2 -/- 20 c.3912C>T p.(Asp1304=) Homo no . -



Screenings


AscendingScreening ID     

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Technique     

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Remarks     

Date of test     

Type of test     

Genes screened     

Variants found     

Owner     
0000001522 DNA CNV;SEQ-NG IACA - 7-may-2019 Multigenetic panel - 26 Silvina Sisterna-Hospital de Comunidad