Variant #0000346782 (NC_000023.10:g.103041396T>C, NM_000533.3:c.194T>C (PLP1))

Chromosome X
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.103041396T>C
DNA change (hg38) g.103786467T>C
Published as PLP1(NM_000533.3):c.194T>C (p.(Ile65Thr)), PLP1(NM_001128834.2):c.194T>C (p.I65T)
ISCN -
DB-ID PLP1_000034 See all 3 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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLP1 NM_000533.3 -?/. - c.194T>C r.(?) p.(Ile65Thr)


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