Variant #0000912687 (NC_000007.13:g.150697687G>C, NM_000603.4:c.1233G>C (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.150697687G>C
DNA change (hg38) -
Published as NOS3(NM_000603.5):c.1233G>C (p.Q411H)
ISCN -
DB-ID ATG9B_000017
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) 3.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOS3 NM_000603.4 ?/. - c.1233G>C r.(?) p.(Gln411His)
ATG9B NM_173681.5 ?/. - c.*13336C>G r.(=) p.(=)


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