Variant #0000332086 (NC_000008.10:g.30700839_30700840del, NM_031271.3:c.5699_5700del (TEX15))

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.30700839_30700840del
DNA change (hg38) g.30843323_30843324del
Published as TEX15(NM_001350162.2):c.6848_6849delGA (p.R2283Nfs*22), TEX15(NM_031271.3):c.5699_5700del (p.?)
ISCN -
DB-ID TEX15_000003 See all 2 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TEX15 NM_031271.3 ?/. - c.5699_5700del r.(?) p.(Arg1900AsnfsTer22)


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