Variant #0000980455 (NC_000012.11:g.7084922C>G, NM_006331.7:c.685C>G (EMG1))

Chromosome 12
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.7084922C>G
DNA change (hg38) -
Published as EMG1(NM_006331.8):c.683C>G (p.(Thr228Ser))
ISCN -
DB-ID EMG1_000020
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHB2 NM_001144831.1 ?/. - c.-5216G>C r.(?) p.(=)
LPCAT3 NM_005768.5 ?/. - c.*1144G>C r.(=) p.(=)
EMG1 NM_006331.7 ?/. - c.685C>G r.(?) p.?


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