Variant #0000656295 (NC_000009.11:g.139371940G>A, NM_014866.1:c.128C>T (SEC16A))

Chromosome 9
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.139371940G>A
DNA change (hg38) g.136477488G>A
Published as SEC16A(NM_014866.1):c.128C>T (p.P43L)
ISCN -
DB-ID C9orf163_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) 0.00018 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 2020-03-23 16:13:27 +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     
SEC16A NM_014866.1 ?/. - c.128C>T r.(?) p.(Pro43Leu)
C9orf163 NM_152571.2 ?/. - c.-6961G>A r.(?) p.(=)


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