Variant #0000893014 (NC_000016.9:g.4933975G>T, NM_032569.3:c.-36709C>A (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.4933975G>T
DNA change (hg38) -
Published as PPL(NM_002705.5):c.4681C>A (p.L1561M)
ISCN -
DB-ID GLYR1_000020
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 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPL NM_002705.4 ?/. - c.4681C>A r.(?) p.(Leu1561Met)
UBN1 NM_016936.3 ?/. - c.*3842G>T r.(=) p.(=)
GLYR1 NM_032569.3 ?/. - c.-36709C>A r.(?) p.(=)


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