Variant #0001053042 (NC_000008.10:g.74888616dup, NM_017866.5:c.100dup (TMEM70))

Chromosome 8
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.74888616dup
DNA change (hg38) -
Published as TMEM70(NM_017866.6):c.100dup (p.(Ala34Glyfs*54))
ISCN -
DB-ID TCEB1_000003
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TCEB1 NM_005648.3 ?/. - c.-4353dup r.(?) p.(=)
TMEM70 NM_017866.5 ?/. - c.100dup r.(?) p.(Ala34Glyfs*54)


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