Variant #0000998055 (NC_000010.10:g.102765312_102765332dup, NM_001195263.1:c.*2893_*2913dup (PDZD7))

Chromosome 10
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.102765312_102765332dup
DNA change (hg38) -
Published as LZTS2(NM_032429.2):c.1166_1186dupTGCTGCAGCTGCAGGTGTTCC (p.(Leu389_Phe395dup))
ISCN -
DB-ID LZTS2_000043
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
PDZD7 NM_001195263.1 ?/. - c.*2893_*2913dup r.(=) p.(=) -
LZTS2 NM_032429.2 ?/. - c.1166_1186dup r.(?) p.(Leu389_Phe395dup) -


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