Variant #0000851994 (NC_000008.10:g.74888546_74888547dup, NM_017866.5:c.30_31dup (TMEM70))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.74888546_74888547dup
DNA change (hg38) -
Published as TMEM70(NM_017866.6):c.30_31dupGG (p.A11Gfs*40)
ISCN -
DB-ID TCEB1_000002
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TCEB1 NM_005648.3 +/. - c.-4285_-4284dup r.(?) p.(=)
TMEM70 NM_017866.5 +/. - c.30_31dup r.(?) p.(Ala11Glyfs*40)


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