Variant #0001050314 (NC_000001.10:g.156146546C>T, NM_001193301.1:c.2044C>T (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.156146546C>T
DNA change (hg38) -
Published as SEMA4A(NM_022367.4):c.2044C>T (p.(Pro682Ser))
ISCN -
DB-ID SEMA4A_000001 See all 5 reported entries
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) 0.00946 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SEMA4A NM_001193301.1 ?/. - c.2044C>T r.(?) p.(Pro682Ser)
SEMA4A NM_022367.3 ?/. - c.2044C>T r.(?) p.(Pro682Ser)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.