Variant #0000950031 (NC_000012.11:g.7244042C>T, NC_000012.11(NM_001733.4):c.231+6G>A (C1R))

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.7244042C>T
DNA change (hg38) -
Published as C1R(NM_001354346.2):c.273+6G>A, C1R(NM_001733.7):c.231+6G>A
ISCN -
DB-ID C1R_000007 See all 2 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) 0.00088 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1R NM_001733.4 -/. - c.231+6G>A r.(=) p.(=)
C1RL NM_016546.2 -/. - c.*4945G>A r.(=) p.(=)


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