Variant #0000558294 (NC_000016.9:g.4935806G>A, NM_032569.3:c.-38540C>T (GLYR1))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.4935806G>A
DNA change (hg38) g.4885805G>A
Published as PPL(NM_002705.5):c.2850C>T (p.F950=)
ISCN -
DB-ID GLYR1_000009
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) 0.0001 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-09 12:01:13 +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.2850C>T r.(?) p.(Phe950=)
UBN1 NM_016936.3 -?/. - c.*5673G>A r.(=) p.(=)
GLYR1 NM_032569.3 -?/. - c.-38540C>T r.(?) p.(=)


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