Variant #0000295718 (NC_000001.10:g.156146669C>T, NM_001193301.1:c.2167C>T (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.156146669C>T
DNA change (hg38) g.156176878C>T
Published as SEMA4A(NM_001370571.1):c.1660C>T (p.R554C), SEMA4A(NM_022367.4):c.2167C>T (p.R723C)
ISCN -
DB-ID SEMA4A_000021
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) 0.00547 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.2167C>T r.(?) p.(Arg723Cys)
SEMA4A NM_022367.3 -?/. - c.2167C>T r.(?) p.(Arg723Cys)


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