Variant #0000807422 (NC_000016.9:g.4935138_4935149del, NM_032569.3:c.-37878_-37867del (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.4935138_4935149del
DNA change (hg38) -
Published as PPL(NM_002705.4):c.3512_3523del (p.(Gln1171_Val1174del))
ISCN -
DB-ID GLYR1_000017
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PPL NM_002705.4 ?/. - c.3512_3523del r.(?) p.(Gln1171_Val1174del)
UBN1 NM_016936.3 ?/. - c.*5005_*5016del r.(=) p.(=)
GLYR1 NM_032569.3 ?/. - c.-37878_-37867del r.(?) p.(=)


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