Variant #0000254822 (NC_000010.10:g.102775504A>G, NM_001195263.1:c.1638T>C (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.102775504A>G
DNA change (hg38) g.101015747A>G
Published as PDZD7(NM_001195263.1):c.1638T>C (p.N546=)
ISCN -
DB-ID PDZD7_000024
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) 8.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-29 10:21:12 +02:00 (CEST)
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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.1638T>C r.(?) p.(Asn546=) -
LZTS2 NM_032429.2 -?/. - c.*8579A>G r.(=) p.(=) -


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