Variant #0000993095 (NC_000002.11:g.97526602C>T, NM_017789.4:c.2263G>A (SEMA4C))

Chromosome 2
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.97526602C>T
DNA change (hg38) -
Published as SEMA4C(NM_017789.4):c.2263G>A (p.(Gly755Ser))
ISCN -
DB-ID ANKRD39_000002
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) 5.0E-5 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKRD39 NM_016466.5 -?/. - c.-2878G>A r.(?) p.(=)
SEMA4C NM_017789.4 -?/. - c.2263G>A r.(?) p.(Gly755Ser)


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