Varaico: Literature-Extracted Genetic Variants

Gene:MEN1
Variant:p.P67L

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.P67L
c.200C>T
Surrounding Variants
1 paper
NM_001370259.2
p.P67R
c.200C>G
1 paper
NM_001370259.2
p.P67insFs
c.200_201insG
1 paper
NM_001370259.2
p.P67insFs
c.200_201ins5
3 papers
NM_001370259.2
p.P67H
c.200C>A
2 papers
NM_001370259.2
p.P67S
c.199C>T
1 paper
NM_001370259.2
p.P67A
c.199C>G
8 papers
NM_001370259.2
p.S66_P67insFs
c.196_200dup5
1 paper
NM_001370259.2
p.Q64_P67insFs
c.191_200dup10
2 papers
NM_001370259.2
p.P67fs
c.199_200fs
1 paper
NM_001370259.2
p.S66_P67Fs
c.196_201delinsTFs
1 paper
NM_001370259.2
p.A68P
c.202G>C
1 paper
NM_001370259.2
p.A68T
c.202G>A
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."