Variant #0000687903 (NC_000001.10:g.156132837A>C, NM_001193301.1:c.1086A>C (SEMA4A))

Chromosome 1
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.156132837A>C
DNA change (hg38) -
Published as SEMA4A(NM_001193300.1):c.1086A>C (p.S362=)
ISCN -
DB-ID SEMA4A_000052
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) 0.00019 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 2020-09-15 15:50:26 +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.1086A>C r.(?) p.(Ser362=)
SEMA4A NM_022367.3 -?/. - c.1086A>C r.(?) p.(Ser362=)


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