Variant #0000535656 (NC_000009.11:g.103062940dup, NM_014425.3:c.3182dup (INVS))

Chromosome 9
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.103062940dup
DNA change (hg38) g.100300658dup
Published as INVS(NM_014425.5):c.3182dupA (p.N1061Kfs*20)
ISCN -
DB-ID TEX10_000015
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INVS NM_014425.3 ?/. - c.3182dup r.(?) p.(Asn1061LysfsTer20)
TEX10 NM_017746.3 ?/. - c.*1538dup r.(?) p.(=)


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