Variant #0000329010 (NC_000022.10:g.38483171_38483179dup, NM_025045.4:c.1216_1224dup (BAIAP2L2))

Chromosome 22
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.38483171_38483179dup
DNA change (hg38) g.38087164_38087172dup
Published as BAIAP2L2(NM_025045.4):c.1224_1225insTCCCCCATG (p.(Ser406_Met408dup))
ISCN -
DB-ID BAIAP2L2_000001
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +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     
SLC16A8 NM_013356.2 ?/. - c.-4134_-4126dup r.(?) p.(=)
BAIAP2L2 NM_025045.4 ?/. - c.1216_1224dup r.(?) p.(Ser406_Met408dup)


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