Variant #0000305823 (NC_000006.11:g.144263781G>A, NM_001080951.1:c.172C>T (PLAGL1))

Chromosome 6
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.144263781G>A
DNA change (hg38) g.143942644G>A
Published as PLAGL1(NM_001289045.1):c.172C>T (p.P58S)
ISCN -
DB-ID PLAGL1_000008
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZC2HC1B NM_001013623.2 ?/. - c.*4517G>A r.(=) p.(=)
PLAGL1 NM_001080951.1 ?/. - c.172C>T r.(?) p.(Pro58Ser)


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