Variant #0000654124 (NC_000001.10:g.92737025A>C, NM_053274.2:c.920T>G (GLMN))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.92737025A>C
DNA change (hg38) g.92271468A>C
Published as GLMN(NM_053274.3):c.920T>G (p.L307*)
ISCN -
DB-ID GLMN_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 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPAP2 NM_024813.2 +/. - c.-27606A>C r.(?) p.(=)
GLMN NM_053274.2 +/. - c.920T>G r.(?) p.(Leu307Ter)


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