Variant #0000129157 (NC_000014.8:g.?)

Individual ID 00080115
Chromosome 14
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.?
DNA change (hg38) -
Published as -
ISCN -
DB-ID SERPINA1_000009 See all 83 reported entries
Variant remarks -
Reference PubMed: Sachwitz 2016, for EUCID-SRS consortium
ClinVar ID -
dbSNP ID -
Origin Somatic
Segregation -
Frequency -
Re-site -
VIP -
Methylation loss of methylation MEG3/DLK1 IG-DMR, MEG3:TSS-DMR, normal methylation H19/IGF2:IG-DMR, KCNQ1OT1:TSS-DMR
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Zeynep Tümer
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2016-09-01 17:30:25 +02:00 (CEST)
Date last edited 2020-10-01 16:53:33 +02:00 (CEST)




Variant on transcripts

Stop! No variants on transcripts found!



Screenings


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Owner     
0000080208 DNA MLPA-ms ; PEms - methylation-sensitive single-nucleotide primer extension - 1 Zeynep Tümer


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