Varaico: Literature-Extracted Genetic Variants

Gene:MN1
Variant:p.P667H

MN1

274 papers

RefSeq Summary

Meningioma 1 (MN1) contains two sets of CAG repeats. It is disrupted by a balanced translocation (4;22) in a meningioma, and its inactivation may contribute to meningioma 32 pathogenesis. [provided by...

Gene Aliases

HGNC Name

MN1 proto-oncogene, transcriptional regulator

HGNC Previous Symbol

MGCR

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
1 paper
NM_002430.3
p.P667H
c.2000C>A
Surrounding Variants
1 paper
NM_002430.3
p.P668L
c.2003C>T
6 papers
NM_002430.3
p.S672L
c.2015C>T
1 paper
NM_002430.3
p.D660D
c.1980C>T
2 papers
NM_002430.3
p.P658L
c.1973C>T
1 paper
NM_002430.3
p.M686T
c.2057T>C
1 paper
NM_002430.3
p.R646S
c.1938G>T
1 paper
NM_002430.3
p.R646S
c.1938G>C
1 paper
NM_002430.3
p.R645H
c.1934G>A
1 paper
NM_002430.3
p.R645C
c.1933C>T
1 paper
NM_002430.3
p.P638L
c.1913C>T
1 paper
NM_002430.3
p.P698P
c.2094G>A
1 paper
NM_002430.3
p.A630V
c.1889C>T
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