Variant #0000883556 (NC_000001.10:g.6537571_6537577del, NC_000001.10(NM_020631.4):c.43+14_43+20del (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.6537571_6537577del
DNA change (hg38) -
Published as PLEKHG5(NM_198681.3):c.274+14_274+20delGGAGCCG, PLEKHG5(NM_198681.4):c.43+14_43+20delGGAGCCG
ISCN -
DB-ID PLEKHG5_000033 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:01:21 +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.43+14_43+20del r.(=) p.(=)
TNFRSF25 NM_148965.1 -?/. - c.-11408_-11402del r.(?) p.(=)


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