Variant #0000998054 (NC_000010.10:g.102752966A>G, NM_001195263.1:c.*15258T>C (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.102752966A>G
DNA change (hg38) -
Published as C10ORF2(NM_021830.4):c.1754A>G (p.(Asn585Ser)), TWNK(NM_021830.5):c.1754A>G (p.N585S)
ISCN -
DB-ID C10orf2_000073 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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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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.*15258T>C r.(=) p.(=) -
C10orf2 NM_021830.4 +?/. - c.1754A>G r.(?) p.(Asn585Ser) -
LZTS2 NM_032429.2 +?/. - c.-4068A>G r.(?) p.(=) -


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