Variant #0000503787 (NC_000001.10:g.156132763G>A, NM_001193301.1:c.1012G>A (SEMA4A))

Chromosome 1
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.156132763G>A
DNA change (hg38) g.156162972G>A
Published as SEMA4A(NM_022367.4):c.1012G>A (p.V338I)
ISCN -
DB-ID SEMA4A_000039
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) 0 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEMA4A NM_001193301.1 ?/. - c.1012G>A r.(?) p.(Val338Ile)
SEMA4A NM_022367.3 ?/. - c.1012G>A r.(?) p.(Val338Ile)


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