Variant #0000549104 (NC_000012.11:g.7080187C>G, NM_006331.7:c.101C>G (EMG1))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7080187C>G
DNA change (hg38) g.6971024C>G
Published as EMG1(NM_001320049.1):c.101C>G (p.(Ala34Gly)), EMG1(NM_006331.7):c.101C>G (p.A34G)
ISCN -
DB-ID EMG1_000003 See all 2 reported entries
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) 0.03052 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHB2 NM_001144831.1 -/. - c.-481G>C r.(?) p.(=)
LPCAT3 NM_005768.5 -/. - c.*5879G>C r.(=) p.(=)
EMG1 NM_006331.7 -/. - c.101C>G r.(?) p.(Ala34Gly)


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