Variant #0000805013 (NC_000011.9:g.134022886A>G, NM_032801.4:c.*3810A>G (JAM3))

Chromosome 11
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.134022886A>G
DNA change (hg38) -
Published as NCAPD3(NM_015261.2):c.4450T>C (p.C1484R)
ISCN -
DB-ID JAM3_000027
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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     
JAM3 NM_001205329.1 -?/. - c.*3810A>G r.(=) p.(=)
NCAPD3 NM_015261.2 -?/. - c.4450T>C r.(?) p.(Cys1484Arg)
JAM3 NM_032801.4 -?/. - c.*3810A>G r.(=) p.(=)


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