Variant #0000331650 (NC_000007.13:g.77762324_77762341dup, NM_012301.3:c.3079_3096dup (MAGI2))

Chromosome 7
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.77762324_77762341dup
DNA change (hg38) g.78133007_78133024dup
Published as MAGI2(NM_012301.3):c.3096_3097insATGGCGCAGCAGAGTCCC (p.(Met1027_Pro1032dup))
ISCN -
DB-ID MAGI2_000022
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MAGI2 NM_012301.3 ?/. - c.3079_3096dup r.(?) p.(Met1027_Pro1032dup)


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