Variant #0000724235 (NC_000012.11:g.7242010G>C, NM_001733.4:c.647C>G (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.7242010G>C
DNA change (hg38) -
Published as C1R(NM_001354346.1):c.689C>G (p.P230R), C1R(NM_001354346.2):c.689C>G (p.P230R)
ISCN -
DB-ID C1R_000005 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) 0.00061 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1R NM_001733.4 -?/. - c.647C>G r.(?) p.(Pro216Arg)
C1RL NM_016546.2 -?/. - c.*6977C>G r.(=) p.(=)


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