Variant #0001005125 (NC_000019.9:g.54972093G>C, NM_052925.2:c.2388G>C (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.54972093G>C
DNA change (hg38) -
Published as LENG8(NM_052925.2):c.2388G>C (p.(Gln796His))
ISCN -
DB-ID CDC42EP5_000007
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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LENG8 NM_052925.2 -?/. - c.2388G>C r.(?) p.(Gln796His)
CDC42EP5 NM_145057.2 -?/. - c.*4192C>G r.(=) p.(=)
LENG9 NM_198988.1 -?/. - c.*1177C>G r.(=) p.(=)


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