Variant #0000679641 (NC_000012.11:g.7177172C>G, NM_001734.3:c.1284C>G (C1S))

Chromosome 12
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.7177172C>G
DNA change (hg38) -
Published as C1S(NM_001734.3):c.1284C>G (p.P428=), C1S(NM_001734.5):c.1284C>G (p.P428=), C1S(NM_201442.3):c.1284C>G (p.P428=)
ISCN -
DB-ID C1S_000003 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) 0.00089 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1S NM_001734.3 -?/. - c.1284C>G r.(?) p.(Pro428=)


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