Variant #0000857584 (NC_000001.10:g.6528159C>G, NM_020631.4:c.2737G>C (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.6528159C>G
DNA change (hg38) -
Published as PLEKHG5(NM_198681.3):c.2968G>C (p.G990R), PLEKHG5(NM_198681.4):c.2737G>C (p.G913R)
ISCN -
DB-ID ESPN_000072 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.2737G>C r.(?) p.(Gly913Arg)
ESPN NM_031475.2 ?/. - c.*7953C>G r.(=) p.(=)
TNFRSF25 NM_148965.1 ?/. - c.-1992G>C r.(?) p.(=)


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