Variant #0000223295 (NC_000005.9:g.155771458G>T, NC_000005.9(NM_000337.5):c.4-41G>T (SGCD))

Chromosome 5
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.155771458G>T
DNA change (hg38) g.156344448G>T
Published as -
ISCN -
DB-ID SGCD_000035
Variant remarks -
Reference from website {DBsub-Emory}
ClinVar ID -
dbSNP ID -
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00895 View details
Owner Madhuri Hegde
Database submission license No license selected
Created by Madhuri Hegde
Date created 2012-10-26 15:20:11 +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     
SGCD NM_000337.5 ?/. 2i c.4-41G>T r.(?) p.(=)


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