Variant #0000329381 (NC_000003.11:g.48474581A>C, NM_002673.4:c.-3979T>G (PLXNB1))

Chromosome 3
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.48474581A>C
DNA change (hg38) g.48433171A>C
Published as CCDC51(NM_001256964.1):c.478-5T>G (p.?)
ISCN -
DB-ID CCDC51_000001
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLXNB1 NM_002673.4 ?/. - c.-3979T>G r.(?) p.(=)
CCDC51 NM_024661.3 ?/. - c.478-5T>G r.spl? p.?


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