Variant #0000297101 (NC_000008.10:g.145047609_145047611del, NC_000008.10(NM_000445.3):c.193+1735_193+1737del (PLEC))

Chromosome 8
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.145047609_145047611del
DNA change (hg38) g.143973441_143973443del
Published as PLEC(NM_201378.4):c.31_33delTTC (p.F11del)
ISCN -
DB-ID PLEC_000228
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLEC NM_000445.3 ?/. - c.193+1735_193+1737del r.(=) p.(=)
PARP10 NM_032789.3 ?/. - c.*4042_*4044del r.(=) p.(=)
PLEC NM_201384.1 ?/. - c.-33981_-33979del r.(?) p.(=)


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