Variant #0000534146 (NC_000008.10:g.145009179G>A, NM_000445.3:c.906C>T (PLEC))

Chromosome 8
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.145009179G>A
DNA change (hg38) g.143935011G>A
Published as PLEC(NM_201380.4):c.1236C>T (p.N412=)
ISCN -
DB-ID PLEC_000529
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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.906C>T r.(?) p.(Asn302=)
PLEC NM_201384.1 -?/. - c.825C>T r.(?) p.(Asn275=)


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