Variant #0000331152 (NC_000006.11:g.107955945_107955953dup, NM_018013.3:c.1897_1905dup (SOBP))

Chromosome 6
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.107955945_107955953dup
DNA change (hg38) g.107634741_107634749dup
Published as SOBP(NM_018013.3):c.1885_1886insGCCCCCCGG (p.(Ser629_Pro630insProProGly))
ISCN -
DB-ID SOBP_000004
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOBP NM_018013.3 ?/. - c.1897_1905dup r.(?) p.(Pro633_Gly635dup)


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