Variant #0000321738 (NC_000010.10:g.102753137A>G, NM_001195263.1:c.*15087T>C (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.102753137A>G
DNA change (hg38) g.100993380A>G
Published as C10orf2(NM_001163812.1):c.*220A>G (p.(=))
ISCN -
DB-ID C10orf2_000026
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) 2.0E-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 2018-01-15 20:58:59 +01:00 (CET)
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.*15087T>C r.(=) p.(=) -
C10orf2 NM_021830.4 ?/. - c.1925A>G r.(?) p.(Lys642Arg) -
LZTS2 NM_032429.2 ?/. - c.-3897A>G r.(?) p.(=) -


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