Varaico: Literature-Extracted Genetic Variants

Gene:MEN1
Variant:p.R92C

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.R92C
c.274C>T
Surrounding Variants
2 papers
NM_001370259.2
p.R92G
c.274C>G
1 paper
NM_001370259.2
p.R92S
c.274C>A
1 paper
NM_001370259.2
p.Y90_A91delFs
c.270_273del4
1 paper
NM_001370259.2
p.R92L
c.275G>T
2 papers
NM_001370259.2
p.R92H
c.275G>A
1 paper
NM_001370259.2
p.R92delFs
c.274delG
1 paper
NM_001370259.2
p.L83_A91delFs
c.248_272del25
4 papers
NM_001370259.2
p.A91V
c.272C>T
1 paper
NM_001370259.2
p.R92_F93insFs
c.276_277insG
1 paper
NM_001370259.2
p.A91insFs
c.272_273insG
1 paper
NM_001370259.2
p.R92fs
c.274_275fs
1 paper
NM_001370259.2
p.R92_F93insFs
c.276_277insA
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