Variant #0000609123 (NC_000004.11:g.17910762A>C, NM_153686.7:c.637T>G (LCORL))

Chromosome 4
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.17910762A>C
DNA change (hg38) g.17909139A>C
Published as LCORL(NM_153686.8):c.637T>G (p.L213V)
ISCN -
DB-ID LCORL_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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 14:54:23 +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     
NCAPG NM_022346.4 ?/. - c.*65714A>C r.(=) p.(=)
LCORL NM_153686.7 ?/. - c.637T>G r.(?) p.(Leu213Val)


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