Variant #0000307998 (NC_000007.13:g.94252709T>C, NM_003919.2:c.391A>G (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.94252709T>C
DNA change (hg38) g.94623397T>C
Published as SGCE(NM_001099400.1):c.391A>G (p.(Ile131Val)), SGCE(NM_001099401.1):c.391A>G (p.I131V), SGCE(NM_003919.3):c.391A>G (p.I131V)
ISCN -
DB-ID SGCE_000071 See all 3 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) 0.00018 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCE NM_003919.2 ?/. - c.391A>G r.(?) p.(Ile131Val)


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