Variant #0001066407 (NC_000016.9:g.4937182C>G, NM_032569.3:c.-39916G>C (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.4937182C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID GLYR1_000027
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) 0.00025 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +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.2561G>C r.(?) p.(Arg854Thr)
UBN1 NM_016936.3 ?/. - c.*7049C>G r.(=) p.(=)
GLYR1 NM_032569.3 ?/. - c.-39916G>C r.(?) p.(=)


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