Variant #0000292127 (NC_000023.10:g.63488523_63488524del, NM_017677.3:c.2008_2009del (MTMR8))

Chromosome X
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.63488523_63488524del
DNA change (hg38) g.64268643_64268644del
Published as MTMR8(NM_017677.3):c.2008_2009delTT (p.L670Gfs*4)
ISCN -
DB-ID MTMR8_000007
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-20 10:51:09 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTMR8 NM_017677.3 ?/. - c.2008_2009del r.(?) p.(Leu670GlyfsTer4)


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