Variant #0000723314 (NC_000011.9:g.134022852_134022853insGT, NM_015261.2:c.4484_4485insCA (NCAPD3))

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.134022852_134022853insGT
DNA change (hg38) -
Published as NCAPD3(NM_015261.2):c.4484_4485insCA (p.K1495Nfs*62)
ISCN -
DB-ID JAM3_000022
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 2021-02-08 18:36:18 +01:00 (CET)
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.*3776_*3777insGT r.(=) p.(=)
NCAPD3 NM_015261.2 ?/. - c.4484_4485insCA r.(?) p.(Lys1495Asnfs*62)
JAM3 NM_032801.4 ?/. - c.*3776_*3777insGT r.(=) p.(=)


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