Variant #0000534869 (NC_000008.10:g.43014187C>T, NM_152419.2:c.493C>T (HGSNAT))

Chromosome 8
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.43014187C>T
DNA change (hg38) g.43159044C>T
Published as HGSNAT(NM_152419.2):c.493C>T (p.(Pro165Ser)), HGSNAT(NM_152419.3):c.493C>T (p.P165S)
ISCN -
DB-ID HGSNAT_000108 See all 3 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) 8.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HGSNAT NM_152419.2 ?/. - c.493C>T r.(?) p.(Pro165Ser)


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