Variant #0000608384 (NC_000003.11:g.154834480del, NM_007289.2:c.467del (MME))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.154834480del
DNA change (hg38) g.155116691del
Published as MME(NM_007288.3):c.467delC (p.P156Lfs*14), MME(NM_007289.3):c.467delC (p.P156Lfs*14), MME(NM_007289.4):c.467delC (p.P156Lfs*14)
ISCN -
DB-ID MME_000023 See all 27 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +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.467del r.(?) p.(Pro156LeufsTer14)


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