Variant #0000534161 (NC_000008.10:g.145024459A>G, NC_000008.10(NM_000445.3):c.194-11599T>C (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.145024459A>G
DNA change (hg38) g.143950291A>G
Published as PLEC(NM_201380.2):c.416T>C (p.(Val139Ala)), PLEC(NM_201380.4):c.416T>C (p.V139A)
ISCN -
DB-ID PLEC_000538 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) 0.00015 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.194-11599T>C r.(=) p.(=)
PLEC NM_201384.1 -?/. - c.-10830T>C r.(?) p.(=)


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