Variant #0000851728 (NC_000007.13:g.94285300A>C, NC_000007.13(NM_003919.2):c.109+2T>G (SGCE))

Chromosome 7
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.94285300A>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID PEG10_000006
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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 15:40:45 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCE NM_003919.2 +/. - c.109+2T>G r.spl? p.?
PEG10 NM_015068.3 +/. - c.-816A>C r.(?) p.(=)


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