Variant #0000997660 (NC_000009.11:g.139347953G>A, NM_014866.1:c.6086C>T (SEC16A))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.139347953G>A
DNA change (hg38) -
Published as SEC16A(NM_014866.1):c.6086C>T (p.(Pro2029Leu))
ISCN -
DB-ID C9orf163_000027
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) 0.00046 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 2024-08-28 13:16:32 +02:00 (CEST)
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.6086C>T r.(?) p.(Pro2029Leu)
C9orf163 NM_152571.2 -?/. - c.-30948G>A r.(?) p.(=)


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