Variant #0000991477 (NC_000001.10:g.92712203C>G, NM_053274.2:c.1669G>C (GLMN))

Chromosome 1
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.92712203C>G
DNA change (hg38) -
Published as GLMN(NM_053274.2):c.1669G>C (p.(Val557Leu))
ISCN -
DB-ID C1orf146_000007
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 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1orf146 NM_001012425.1 ?/. - c.*972C>G r.(=) p.(=)
RPAP2 NM_024813.2 ?/. - c.-52428C>G r.(?) p.(=)
GLMN NM_053274.2 ?/. - c.1669G>C r.(?) p.(Val557Leu)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.