Varaico: Literature-Extracted Genetic Variants

Gene:MEN1
Variant:p.R29G

MEN1

1,357 papers

RefSeq Summary

This gene encodes menin, a tumor suppressor associated with a syndrome known as multiple endocrine neoplasia type 1. Menin is a scaffold protein that functions in histone modification and epigenetic g...

Pfam Domains

Meninaa 1–146UCSCMenin
Meninaa 1–510UCSCMenin
Meninaa 364–552UCSCMenin
Meninaa 515–608UCSCMenin

Gene Aliases

HGNC Name

menin 1

HGNC Previous Name

multiple endocrine neoplasia I

Papers
RefSeq ID
Protein change
DNA change
Selected Variant
2 papers
NM_001370259.2
p.R29G
c.85C>G
Surrounding Variants
13 papers
NM_001370259.2
p.R29*
c.85C>T
1 paper
NM_001370259.2
p.S15_G28del14
c.43_83del42
5 papers
NM_001370259.2
p.R29Q
c.86G>A
1 paper
NM_001370259.2
p.R29delFs
c.85delG
2 papers
NM_001370259.2
p.G28delFs
c.82delC
5 papers
NM_001370259.2
p.G28A
c.83G>C
1 paper
NM_001370259.2
p.G28D
c.83G>A
1 paper
NM_001370259.2
p.G28delins
c.82_83delinsAA
1 paper
NM_001370259.2
p.R29R
c.87A>T
1 paper
NM_001370259.2
p.G28_R29delFs
c.82_85del4
7 papers
NM_001370259.2
p.E30*
c.88G>T
1 paper
NM_001370259.2
p.G28R
c.82G>C
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