Variant #0000332956 (NC_000009.11:g.140317997G>A, NM_017820.3:c.-479C>T (EXD3))

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.140317997G>A
DNA change (hg38) g.137423545G>A
Published as NOXA1(NM_001256067.1):c.16G>A (p.(Asp6Asn))
ISCN -
DB-ID ENTPD8_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     
NOXA1 NM_001256067.1 ?/. - c.16G>A r.(?) p.(Asp6Asn)
EXD3 NM_017820.3 ?/. - c.-479C>T r.(?) p.(=)
ENTPD8 NM_198585.2 ?/. - c.*11369C>T r.(=) p.(=)


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