Variant #0000331963 (NC_000007.13:g.150721489C>G, NM_000603.4:c.*10232C>G (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.150721489C>G
DNA change (hg38) g.151024402C>G
Published as ATG9B(NM_173681.5):c.22G>C (p.(Gly8Arg))
ISCN -
DB-ID ATG9B_000001
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) 0.0016 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-23 15:00:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NOS3 NM_000603.4 ?/. - c.*10232C>G r.(=) p.(=)
ABCB8 NM_007188.3 ?/. - c.-4114C>G r.(?) p.(=)
ATG9B NM_173681.5 ?/. - c.22G>C r.(?) p.(Gly8Arg)


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