Variant #0000002712 (NC_000001.11:g.207623026T>C, CR1(NM_000651.6):c.7310T>C)

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg38 / GRCh38) g.207623026T>C
Published as -
Reference Yock-Ping Chow et al.(2017)
DB-ID CR1_000001
dbSNP ID rs773158798
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by MyHVP
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
CR1 NM_000651.6 ?/? - c.7310T>C - r.(?) p.(Leu2437Pro) -