Variant #0000002547 (NC_000001.11:g.13267C>A, NM_000488.3:c.1315C>A (SERPINC1))

Individual ID 00000558
Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.13267C>A
Published as -
Reference A T Norlelawati et al.(2014)dbSNP
DB-ID SERPINC1_000001
dbSNP ID rs1487411568
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-04-04 11:41:38 +08:00 (CST)
Date last edited 2021-09-06 09:33:41 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
SERPINC1 NM_000488.3 +?/. 7 c.1315C>A - r.(?) p.(Pro439Thr) ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000609 DNA PCR;SEQ SERPINC1 1 Nur Aisyah Athirah