Variant #0000726442 (NC_000017.10:g.42085890G>A, NAGS(NM_153006.2):c.1526G>A)

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.42085890G>A
DNA change (hg38) -
Published as NAGS(NM_153006.2):c.1526G>A (p.R509Q)
ISCN -
DB-ID NAGS_000028 See all 2 reported entries
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PYY NM_004160.4 ?/. - c.-4594C>T r.(?) p.(=)
TMEM101 NM_032376.2 ?/. - c.*3406C>T r.(=) p.(=)
NAGS NM_153006.2 ?/. - c.1526G>A r.(?) p.(Arg509Gln)