Variant #0000549102 (NC_000012.11:g.7079405C>T, NM_006331.7:c.-682C>T (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.7079405C>T
DNA change (hg38) g.6970242C>T
Published as PHB2(NM_001144831.1):c.166G>A (p.(Gly56Ser))
ISCN -
DB-ID EMG1_000012
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PHB2 NM_001144831.1 ?/. - c.166G>A r.(?) p.(Gly56Ser)
LPCAT3 NM_005768.5 ?/. - c.*6661G>A r.(=) p.(=)
EMG1 NM_006331.7 ?/. - c.-682C>T r.(?) p.(=)


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