Variant #0000997662 (NC_000009.11:g.139370770T>C, NM_014866.1:c.1298A>G (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.139370770T>C
DNA change (hg38) -
Published as SEC16A(NM_014866.1):c.1298A>G (p.(Asn433Ser))
ISCN -
DB-ID C9orf163_000029
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_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.1298A>G r.(?) p.(Asn433Ser)
C9orf163 NM_152571.2 -?/. - c.-8131T>C r.(?) p.(=)


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