Variant #0000998880 (NC_000011.9:g.134023044G>A, NM_032801.4:c.*3968G>A (JAM3))

Chromosome 11
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.134023044G>A
DNA change (hg38) -
Published as NCAPD3(NM_015261.2):c.4379C>T (p.(Pro1460Leu))
ISCN -
DB-ID JAM3_000035
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) 1.0E-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 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JAM3 NM_001205329.1 ?/. - c.*3968G>A r.(=) p.(=)
NCAPD3 NM_015261.2 ?/. - c.4379C>T r.(?) p.(Pro1460Leu)
JAM3 NM_032801.4 ?/. - c.*3968G>A r.(=) p.(=)


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