Variant #0000538924 (NC_000010.10:g.102771699G>C, NM_001195263.1:c.1916C>G (PDZD7))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.102771699G>C
DNA change (hg38) g.101011942G>C
Published as PDZD7(NM_001195263.2):c.1916C>G (p.A639G)
ISCN -
DB-ID PDZD7_000005 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) 0.00184 View details
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     

P-domain     
PDZD7 NM_001195263.1 -/. - c.1916C>G r.(?) p.(Ala639Gly) -
LZTS2 NM_032429.2 -/. - c.*4774G>C r.(=) p.(=) -


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