Variant #0001072209 (NC_000006.11:g.107955369C>T, NM_018013.3:c.1321C>T (SOBP))

Chromosome 6
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.107955369C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID SOBP_000016 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs201319446
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00123 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-09 17:21:01 +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     
SOBP NM_018013.3 -?/. - c.1321C>T r.(?) p.(Pro441Ser)


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