Variant #0000558293 (NC_000016.9:g.4934357_4934359del, NM_032569.3:c.-37089_-37087del (GLYR1))

Chromosome 16
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.4934357_4934359del
DNA change (hg38) g.4884356_4884358del
Published as PPL(NM_002705.5):c.4301_4303delAAG (p.E1434del)
ISCN -
DB-ID GLYR1_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_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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPL NM_002705.4 ?/. - c.4301_4303del r.(?) p.(Glu1434del)
UBN1 NM_016936.3 ?/. - c.*4224_*4226del r.(=) p.(=)
GLYR1 NM_032569.3 ?/. - c.-37089_-37087del r.(?) p.(=)


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