Variant #0000291005 (NC_000022.10:g.50945401C>A, NM_005138.2:c.*16639G>T (SCO2))

Chromosome 22
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.50945401C>A
DNA change (hg38) g.50506972C>A
Published as LMF2(NM_033200.3):c.158G>T (p.R53L)
ISCN -
DB-ID LMF2_000006
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 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     
SCO2 NM_005138.2 -?/. - c.*16639G>T r.(=) p.(=)
LMF2 NM_033200.2 -?/. - c.158G>T r.(?) p.(Arg53Leu)
NCAPH2 NM_152299.3 -?/. - c.-1366C>A r.(?) p.(=)


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