Variant #0000538932 (NC_000010.10:g.102789780C>T, NM_001195263.1:c.197G>A (PDZD7))

Chromosome 10
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.102789780C>T
DNA change (hg38) g.101030023C>T
Published as PDZD7(NM_001195263.1):c.197G>A (p.R66H)
ISCN -
DB-ID LZTS2_000021
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) 1.0E-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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.197G>A r.(?) p.(Arg66His) -
SFXN3 NM_030971.3 ?/. - c.-1672C>T r.(?) p.(=) -
LZTS2 NM_032429.2 ?/. - c.*22855C>T r.(=) p.(=) -


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