Variant #0000330229 (NC_000005.9:g.194849T>A, NM_052909.3:c.*12411T>A (PLEKHG4B))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.194849T>A
DNA change (hg38) g.194734T>A
Published as LRRC14B(NM_001080478.1):c.926T>A (p.(Leu309Gln))
ISCN -
DB-ID PLEKHG4B_000004
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) 0.00066 View details
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC14B NM_001080478.1 ?/. - c.926T>A r.(?) p.(Leu309Gln)
PLEKHG4B NM_052909.3 ?/. - c.*12411T>A r.(=) p.(=)


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