Variant #0000250143 (NC_000007.13:g.116340086A>G, NM_001127500.1:c.948A>G (MET))

Chromosome 7
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.116340086A>G
DNA change (hg38) g.116700032A>G
Published as MET(NM_000245.2):c.948A>G (p.(Ile316Met)), MET(NM_001127500.3):c.948A>G (p.I316M)
ISCN -
DB-ID MET_000124 See all 2 reported entries
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) 0.00161 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MET NM_000245.2 -/. - c.948A>G r.(?) p.(Ile316Met)
MET NM_001127500.1 -/. - c.948A>G r.(?) p.(Ile316Met)


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