Variant #0000290962 (NC_000019.9:g.54973913C>G, NM_052925.2:c.*1805C>G (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.54973913C>G
DNA change (hg38) g.54462733C>G
Published as LENG9(NM_198988.2):c.863G>C (p.G288A)
ISCN -
DB-ID LENG9_000002
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LENG8 NM_052925.2 -?/. - c.*1805C>G r.(=) p.(=)
CDC42EP5 NM_145057.2 -?/. - c.*2372G>C r.(=) p.(=)
LENG9 NM_198988.1 -?/. - c.863G>C r.(?) p.(Gly288Ala)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.