Varaico: Literature-Extracted Genetic Variants

Gene:MEN1
Variant:p.M558_K559del1

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
3 papers
NM_001370259.2
p.M558_K559del1
c.1673_1675delTCA
Surrounding Variants
1 paper
NM_001370259.2
p.K559insFs
c.1676_1677insG
3 papers
NM_001370259.2
p.K559delFs
c.1676delT
3 papers
NM_001370259.2
p.K559*
c.1675A>T
1 paper
NM_001370259.2
p.G560_M561ins11
c.1678_1682ins33
1 paper
NM_001370259.2
p.G560fs
c.1678_1679fs
3 papers
NM_001370259.2
p.M558K
c.1673T>A
1 paper
NM_001370259.2
p.M558delFs
c.1672delT
2 papers
NM_001370259.2
p.K557del1
c.1669_1670delCTT
1 paper
NM_001370259.2
p.S555_K559delFs
c.1664_1677del14
1 paper
NM_001370259.2
p.G560delFs
c.1679delC
2 papers
NM_001370259.2
p.K557fs
c.1669_1670fs
NM_000244.4
p.K562fs
c.1684_1685fs
1 paper
NM_001370259.2
p.M561fs
c.1681_1682fs
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