Variant #0000721620 (NC_000007.13:g.94285409A>G, NM_003919.2:c.2T>C (SGCE))

Chromosome 7
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.94285409A>G
DNA change (hg38) -
Published as SGCE(NM_001099401.2):c.2T>C (p.M1?)
ISCN -
DB-ID PEG10_000003
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 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
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.2T>C r.(?) p.(Met1?)
PEG10 NM_015068.3 ?/. - c.-707A>G r.(?) p.(=)


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