Variant #0000605904 (NC_000001.10:g.6530744_6530748dup, NC_000001.10(NM_020631.4):c.1543-44_1543-40dup (PLEKHG5))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.6530744_6530748dup
DNA change (hg38) g.6470684_6470688dup
Published as PLEKHG5(NM_198681.4):c.1543-44_1543-40dupCTCCG
ISCN -
DB-ID ESPN_000040
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 14:54:23 +01:00 (CET)
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.1543-44_1543-40dup r.(=) p.(=)
ESPN NM_031475.2 -?/. - c.*10538_*10542dup r.(=) p.(=)
TNFRSF25 NM_148965.1 -?/. - c.-4580_-4576dup r.(?) p.(=)


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