Varaico: Literature-Extracted Genetic Variants

Gene:MEN1
Variant:p.I16_D17insC

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.I16_D17insC
c.46_50ins3
Surrounding Variants
1 paper
NM_001370259.2
p.I16V
c.46A>G
1 paper
NM_001370259.2
p.R14_S15del2
c.40_44del6
1 paper
NM_001370259.2
p.I16T
c.47T>C
1 paper
NM_001370259.2
p.S15S
c.45C>G
2 papers
NM_001370259.2
p.S15fs
c.43_44fs
1 paper
NM_001370259.2
p.I16I
c.48C>T
1 paper
NM_001370259.2
p.S15F
c.44C>T
1 paper
NM_001370259.2
p.S15C
c.44C>G
1 paper
NM_001370259.2
p.I16delFs
c.47delA
1 paper
NM_001370259.2
p.R14insFs
c.41_42dupGC
3 papers
NM_001370259.2
p.S15P
c.43T>C
1 paper
NM_001370259.2
p.R14delFs
c.42delG
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