Variant #0000857589 (NC_000001.10:g.6534519C>A, NM_020631.4:c.431G>T (PLEKHG5))

Chromosome 1
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.6534519C>A
DNA change (hg38) -
Published as PLEKHG5(NM_198681.3):c.662G>T (p.R221L), PLEKHG5(NM_198681.4):c.431G>T (p.R144L)
ISCN -
DB-ID PLEKHG5_000030 See all 2 reported entries
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 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLEKHG5 NM_020631.4 ?/. - c.431G>T r.(?) p.(Arg144Leu)
TNFRSF25 NM_148965.1 ?/. - c.-8352G>T r.(?) p.(=)


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