Variant #0000982533 (NC_000017.10:g.42085048G>A, NM_153006.2:c.1358G>A (NAGS))

Chromosome 17
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.42085048G>A
DNA change (hg38) -
Published as NAGS(NM_153006.3):c.1358G>A (p.(Gly453Asp))
ISCN -
DB-ID NAGS_000056
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PYY NM_004160.4 ?/. - c.-3752C>T r.(?) p.(=)
TMEM101 NM_032376.2 ?/. - c.*4248C>T r.(=) p.(=)
NAGS NM_153006.2 ?/. - c.1358G>A r.(?) p.(Gly453Asp)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.