Variant #0000808922 (NC_000019.9:g.4543920A>C, NM_032108.3:c.2360T>G (SEMA6B))

Chromosome 19
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.4543920A>C
DNA change (hg38) -
Published as SEMA6B(NM_032108.4):c.2360T>G (p.F787C)
ISCN -
DB-ID SEMA6B_000015
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEMA6B NM_032108.3 ?/. - c.2360T>G r.(?) p.(Phe787Cys)
LRG1 NM_052972.2 ?/. - c.-3895T>G r.(?) p.(=)


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