Variant #0000622298 (NC_000009.11:g.91949566_91949567insACC, NM_024077.3:c.1010_1011insACC (SECISBP2))

Chromosome 9
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.91949566_91949567insACC
DNA change (hg38) g.89334651_89334652insACC
Published as SECISBP2(NM_001282690.1):c.806_807insACC (p.V269_S270insP)
ISCN -
DB-ID SECISBP2_000013
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) 0.00013 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
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     
SECISBP2 NM_024077.3 ?/. - c.1010_1011insACC r.(?) p.(Val337_Ser338insPro)


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