Variant #0000508220 (NC_000001.10:g.6533387T>C, NM_020631.4:c.719A>G (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.6533387T>C
DNA change (hg38) g.6473327T>C
Published as PLEKHG5(NM_198681.3):c.950A>G (p.D317G), PLEKHG5(NM_198681.4):c.719A>G (p.D240G)
ISCN -
DB-ID PLEKHG5_000040 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) 0.00036 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 2019-07-18 18:22:55 +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.719A>G r.(?) p.(Asp240Gly)
TNFRSF25 NM_148965.1 ?/. - c.-7220A>G r.(?) p.(=)


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