Variant #0000612237 (NC_000010.10:g.102781620C>T, NM_001195263.1:c.802G>A (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.102781620C>T
DNA change (hg38) g.101021863C>T
Published as PDZD7(NM_001195263.1):c.802G>A (p.D268N)
ISCN -
DB-ID LZTS2_000027
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) 0.0002 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

P-domain     
PDZD7 NM_001195263.1 ?/. - c.802G>A r.(?) p.(Asp268Asn) -
LZTS2 NM_032429.2 ?/. - c.*14695C>T r.(=) p.(=) -


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.