Variant #0000326781 (NC_000019.9:g.54974607C>T, NM_052925.2:c.*2499C>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.54974607C>T
DNA change (hg38) g.54463424C>T
Published as LENG9(NM_198988.1):c.169G>A (p.(Gly57Ser))
ISCN -
DB-ID LENG9_000005
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_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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LENG8 NM_052925.2 -?/. - c.*2499C>T r.(=) p.(=)
CDC42EP5 NM_145057.2 -?/. - c.*1678G>A r.(=) p.(=)
LENG9 NM_198988.1 -?/. - c.169G>A r.(?) p.(Gly57Ser)


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