Variant #0001026231 (NC_000012.11:g.7244286C>T, NC_000012.11(NM_001733.4):c.3-10G>A (C1R))

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.7244286C>T
DNA change (hg38) -
Published as C1R(NM_001354346.1):c.45-10G>A, C1R(NM_001354346.2):c.45-10G>A, C1R(NM_001733.7):c.3-10G>A
ISCN -
DB-ID C1R_000013 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) 0.00082 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 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1R NM_001733.4 -?/. - c.3-10G>A r.(=) p.(=)
C1RL NM_016546.2 -?/. - c.*4701G>A r.(=) p.(=)


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