Variant #0000802995 (NC_000007.13:g.150697616C>T, NM_000603.4:c.1162C>T (NOS3))

Chromosome 7
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.150697616C>T
DNA change (hg38) -
Published as NOS3(NM_000603.4):c.1162C>T (p.R388W), NOS3(NM_000603.5):c.1162C>T (p.R388W)
ISCN -
DB-ID ATG9B_000012 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) 0.0002 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOS3 NM_000603.4 ?/. - c.1162C>T r.(?) p.(Arg388Trp)
ATG9B NM_173681.5 ?/. - c.*13407G>A r.(=) p.(=)


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