Variant #0000543052 (NC_000011.9:g.134014673_134014674insCTT, NC_000011.9(NM_032801.4):c.410-14_410-13insCTT (JAM3))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.134014673_134014674insCTT
DNA change (hg38) g.134144778_134144779insCTT
Published as JAM3(NM_032801.4):c.410-14_410-13insCTT
ISCN -
DB-ID JAM3_000015
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JAM3 NM_001205329.1 -/. - c.257-14_257-13insCTT r.(=) p.(=)
JAM3 NM_032801.4 -/. - c.410-14_410-13insCTT r.(=) p.(=)


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