Variant #0000861794 (NC_000010.10:g.102783263G>A, NM_001195263.1:c.472C>T (PDZD7))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.102783263G>A
DNA change (hg38) -
Published as PDZD7(NM_001195263.1):c.472C>T (p.R158C)
ISCN -
DB-ID LZTS2_000037
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 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 2022-05-09 15:51:19 +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.472C>T r.(?) p.(Arg158Cys) -
LZTS2 NM_032429.2 -?/. - c.*16338G>A r.(=) p.(=) -


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