Variant #0000290961 (NC_000019.9:g.54973325C>T, NM_052925.2:c.*1217C>T (LENG8))

Chromosome 19
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.54973325C>T
DNA change (hg38) g.54462145C>T
Published as LENG9(NM_198988.2):c.1451G>A (p.R484H)
ISCN -
DB-ID LENG9_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) 4.0E-5 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 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     
LENG8 NM_052925.2 -?/. - c.*1217C>T r.(=) p.(=)
CDC42EP5 NM_145057.2 -?/. - c.*2960G>A r.(=) p.(=)
LENG9 NM_198988.1 -?/. - c.1451G>A r.(?) p.(Arg484His)


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