Variant #0000276133 (NC_000012.11:g.7084434T>C, NM_006331.7:c.515T>C (EMG1))

Chromosome 12
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.7084434T>C
DNA change (hg38) g.6975272T>C
Published as EMG1(NM_006331.7):c.515T>C (p.M172T)
ISCN -
DB-ID EMG1_000009
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
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.-4728A>G r.(?) p.(=)
LPCAT3 NM_005768.5 -?/. - c.*1632A>G r.(=) p.(=)
EMG1 NM_006331.7 -?/. - c.515T>C r.(?) p.(Met172Thr)


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