Variant #0000996159 (NC_000007.13:g.12271535_12271536del, NM_018374.3:c.759_760del (TMEM106B))

Chromosome 7
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.12271535_12271536del
DNA change (hg38) -
Published as TMEM106B(NM_001134232.1):c.759_760delTG (p.(Cys253fs))
ISCN -
DB-ID TMEM106B_000006
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM106B NM_018374.3 ?/. - c.759_760del r.(?) p.(Cys253Trpfs*12)


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