Variant #0001000322 (NC_000012.11:g.7177214C>T, NM_001734.3:c.1326C>T (C1S))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7177214C>T
DNA change (hg38) -
Published as C1S(NM_001734.3):c.1326C>T (p.S442=), C1S(NM_001734.5):c.1326C>T (p.S442=), C1S(NM_201442.3):c.1326C>T (p.S442=)
ISCN -
DB-ID C1S_000014 See all 3 reported entries
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) 0.00067 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1S NM_001734.3 -/. - c.1326C>T r.(?) p.(Ser442=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.