Variant #0000703849 (NC_000004.11:g.52895932G>A, NM_000232.4:c.341C>T (SGCB))

Chromosome 4
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.52895932G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID SGCB_000012 See all 97 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs150518260
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00028 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2020-11-09 18:11:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SGCB NM_000232.4 +/. - c.341C>T r.(?) p.(Ser114Phe)


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