Variant #0000996770 (NC_000007.13:g.94285352C>T, NM_003919.2:c.59G>A (SGCE))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.94285352C>T
DNA change (hg38) -
Published as SGCE(NM_003919.2):c.59G>A (p.(Arg20Gln))
ISCN -
DB-ID PEG10_000009
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) 6.0E-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     
SGCE NM_003919.2 -?/. - c.59G>A r.(?) p.(Arg20Gln)
PEG10 NM_015068.3 -?/. - c.-764C>T r.(?) p.(=)


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