Variant #0000298849 (NC_000010.10:g.102770318_102770327del, NM_001195263.1:c.2319_2328del (PDZD7))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.102770318_102770327del
DNA change (hg38) g.101010561_101010570del
Published as PDZD7(NM_001195263.1):c.2319_2328delTAGCCGCAGC (p.S774Vfs*31), PDZD7(NM_001195263.2):c.2319_2328delTAGCCGCAGC (p.S774Vfs*31)
ISCN -
DB-ID PDZD7_000048 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) 0.00026 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     

P-domain     
PDZD7 NM_001195263.1 +?/. - c.2319_2328del r.(?) p.(Ser774ValfsTer31) -
LZTS2 NM_032429.2 +?/. - c.*3393_*3402del r.(=) p.(=) -


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