Varaico: Literature-Extracted Genetic Variants

Gene:MEN1
Variant:p.P32_L36del0

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
1 paper
NM_001370259.2
p.P32_L36del0
c.95_106del12
Surrounding Variants
2 papers
NM_001370259.2
p.L36H
c.107T>A
3 papers
NM_001370259.2
p.L36F
c.106C>T
2 papers
NM_001370259.2
p.V35_L36ins0
c.105_107dupGCT
1 paper
NM_001370259.2
p.V35insFs
c.105dupG
1 paper
NM_001370259.2
p.V35delFs
c.104_105delCA
1 paper
NM_001370259.2
p.D33_V35delFs
c.98_105del8
1 paper
NM_001370259.2
p.L37fs
c.109_110fs
1 paper
NM_001370259.2
p.L37F
c.109C>T
1 paper
NM_001370259.2
p.A24_L36del13
c.70_107del39
1 paper
NM_001370259.2
p.L36insFs
c.108dupC
2 papers
NM_001370259.2
p.L37R
c.110T>G
6 papers
NM_001370259.2
p.L37P
c.110T>C
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