Variant #0000326104 (NC_000019.9:g.7687730T>C, NM_020196.2:c.1289A>G (XAB2))

Chromosome 19
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.7687730T>C
DNA change (hg38) g.7622844T>C
Published as XAB2(NM_020196.2):c.1289A>G (p.(Asp430Gly))
ISCN -
DB-ID XAB2_000002
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) 0.00033 View details
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 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CAMSAP3 NM_001080429.2 ?/. - c.*4787T>C r.(=) p.(=)
XAB2 NM_020196.2 ?/. - c.1289A>G r.(?) p.(Asp430Gly)


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