Variant #0000293650 (NC_000010.10:g.102789821G>A, NM_001195263.1:c.156C>T (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.102789821G>A
DNA change (hg38) g.101030064G>A
Published as PDZD7(NM_001195263.1):c.156C>T (p.N52=), PDZD7(NM_001195263.2):c.156C>T (p.N52=)
ISCN -
DB-ID PDZD7_000036 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) 0.00137 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 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.156C>T r.(?) p.(Asn52=) -
SFXN3 NM_030971.3 -/. - c.-1631G>A r.(?) p.(=) -
LZTS2 NM_032429.2 -/. - c.*22896G>A r.(=) p.(=) -


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