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Varaico: Literature-Extracted Genetic Variants

Include likely false extractions

Gene:IL37

IL37

61 papers

RefSeq Summary

The protein encoded by this gene is a member of the interleukin 1 cytokine family. This cytokine can bind to, and may be a ligand for interleukin 18 receptor (IL18R1/IL-1Rrp). This cytokine also binds...

Pfam Domains

IL1aa 83–203UCSCInterleukin-1 / 18

Gene Aliases

HGNC Name

interleukin 37

HGNC Previous Symbol

IL1F7

Papers

Position

RefSeq ID

Protein change

DNA change

Pfam

gnomAD

1–12 of 164 variants

13 papers

chr2:112913833 A>G

NM_014439.4

p.T42A

c.124A>G

Exome: 70.3% (AC=1025118, hom=364433)Genome: 60.9% (AC=92581, hom=30741)148 overlapping SVs

12 papers

chr2:112913801 G>T

NM_014439.4

p.G31V

c.92G>T

Exome: 70.1% (AC=1021735, hom=363133)Genome: 59.4% (AC=90402, hom=30082)148 overlapping SVs

6 papers

chr2:112917144 A>G

NM_014439.4

p.N54S

c.161A>G

Exome: 7.5% (AC=109664, hom=4704)Genome: 9.7% (AC=14712, hom=936)146 overlapping SVs

6 papers

chr2:112917692 C>T

NM_014439.4

p.P108L

c.323C>T

IL1

Exome: 7.5% (AC=110064, hom=4687)Genome: 9.6% (AC=14674, hom=929)146 overlapping SVs

6 papers

chr2:112918697 A>G

NM_014439.4

p.N182S

c.545A>G

IL1

Exome: 0.0% (AC=39, hom=0)Genome: 0.0% (AC=8, hom=0)146 overlapping SVs

5 papers

chr2:112913054 T>A

NM_014439.4

p.S14S

c.42T>A

exact variant not in gnomAD146 overlapping SVs

5 papers

chr2:112917132 C>G

NM_014439.4

p.P50R

c.149C>G

Exome: 7.5% (AC=109514, hom=4697)Genome: 9.7% (AC=14715, hom=939)146 overlapping SVs

5 papers

chr2:112918642 T>A

NM_014439.4

p.W164R

c.490T>A

IL1

exact variant not in gnomAD146 overlapping SVs

5 papers

chr2:112918642 T>C

NM_014439.4

p.W164R

c.490T>C

IL1

Exome: 7.6% (AC=110522, hom=4704)Genome: 9.7% (AC=14708, hom=937)146 overlapping SVs

4 papers

chr2:112918804 G>A

NM_014439.4

p.D218N

c.652G>A

Exome: 7.6% (AC=110186, hom=4686)Genome: 9.6% (AC=14664, hom=929)146 overlapping SVs

2 papers

chr2:112913801 G>C

NM_014439.4

p.G31A

c.92G>C

Exome: 0.0% (AC=1, hom=0)Genome: n/a148 overlapping SVs

2 papers

chr2:112917153 C>A

NM_014439.4

p.P57Q

c.170C>A

Exome: 0.0% (AC=1, hom=0)Genome: n/a146 overlapping SVs

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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."