Variant #0000321273 (NC_000001.10:g.207818658T>G, NM_000573.3:c.*5904T>G (CR1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.207818658T>G
DNA change (hg38) g.207645313T>G
Published as CR1L(NM_175710.1):c.80T>G (p.(Leu27Arg))
ISCN -
DB-ID CR1L_000001
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) 0.00335 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CR1 NM_000573.3 ?/. - c.*5904T>G r.(=) p.(=)
CR1L NM_175710.1 ?/. - c.80T>G r.(?) p.(Leu27Arg)


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