Variant #0000678325 (NC_000008.10:g.145013583C>T, NC_000008.10(NM_000445.3):c.194-723G>A (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.145013583C>T
DNA change (hg38) -
Published as PLEC(NM_000445.3):c.194-723G>A (p.(=)), PLEC(NM_201384.2):c.47G>A (p.R16Q)
ISCN -
DB-ID PLEC_000536 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) 9.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +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.194-723G>A r.(=) p.(=)
PLEC NM_201384.1 -?/. - c.47G>A r.(?) p.(Arg16Gln)


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