Variant #0000518333 (NC_000003.11:g.154859862A>G, NM_007289.2:c.1040A>G (MME))

Chromosome 3
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.154859862A>G
DNA change (hg38) g.155142073A>G
Published as MME(NM_007289.3):c.1040A>G (p.Y347C), MME(NM_007289.4):c.1040A>G (p.Y347C, p.(Tyr347Cys))
ISCN -
DB-ID MME_000009 See all 5 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) 0.00052 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MME NM_007289.2 ?/. - c.1040A>G r.(?) p.(Tyr347Cys)


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