Variant #0000857587 (NC_000001.10:g.6530697_6530698del, NM_020631.4:c.1549_1550del (PLEKHG5))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.6530697_6530698del
DNA change (hg38) -
Published as PLEKHG5(NM_198681.3):c.1780_1781delTC (p.S594Rfs*137)
ISCN -
DB-ID ESPN_000085
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_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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLEKHG5 NM_020631.4 +?/. - c.1549_1550del r.(?) p.(Ser517Argfs*137)
ESPN NM_031475.2 +?/. - c.*10491_*10492del r.(=) p.(=)
TNFRSF25 NM_148965.1 +?/. - c.-4530_-4529del r.(?) p.(=)


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