49364712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32352228-T-C

http://identifiers.org/hco/10/GRCh38#49364761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32352188-C-A

49364895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32352047-A-G

http://identifiers.org/hco/10/GRCh38#49365066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32351888-C-A

49365066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351888-C-G

49365083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351873-T-C

49365206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351815-G-C

49365206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351815-G-T

49365286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351742-G-T

49365298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351730-T-C

49365310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351717-G-T

49365344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351693-G-T

49365349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351688-A-G

http://identifiers.org/hco/10/GRCh38#49365386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32351649-C-A

49365401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351634-A-G

http://identifiers.org/hco/10/GRCh38#49365425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32351610-C-A

49365425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351610-C-T

49365445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351583-G-A

49365445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351583-G-T

49365453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351575-G-A

49365504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351544-G-A

49365504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351544-G-T

49365511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351537-T-C

49365591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351497-T-C

49365619-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351469-T-A

49365627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351461-T-C

49365635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351453-G-A

49365635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351453-G-T

http://identifiers.org/hco/10/GRCh38#49365682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32351407-C-A

49365682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351407-C-T

http://identifiers.org/hco/10/GRCh38#49365684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32351405-C-A

http://identifiers.org/hco/10/GRCh38#49365691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32351402-C-A

49365691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351402-C-T

49365692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351401-G-A

49365692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351401-G-C

49365692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351401-G-T

http://identifiers.org/hco/10/GRCh38#49365695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32351398-A-C

49365695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351398-A-G

49365729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351341-T-A

49365729-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351341-T-G

49365782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351291-A-G

49365784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351289-G-A

49365812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351267-C-T

http://identifiers.org/hco/10/GRCh38#49365821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32351258-C-A

49365821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351258-C-T

49365850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351201-G-A

49365850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351201-G-T

49365854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351197-C-T

49365972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351078-T-C

49365974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351076-G-A

49365974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351076-G-T

49365978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351072-T-C

49365994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351057-G-A

49365994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351057-G-T

http://identifiers.org/hco/10/GRCh38#49365997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32351054-C-A

49365997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351054-C-T

49366001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351050-G-A

49366001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351050-G-T

http://identifiers.org/hco/10/GRCh38#49366002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32351049-C-A

49366002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32351049-C-T

http://identifiers.org/hco/10/GRCh38#49366071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32350997-A-C

49366073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32350995-G-T

49366094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32350977-C-T

http://identifiers.org/hco/10/GRCh38#49366095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32350976-C-A

49366095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32350976-C-G

49366095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 3 prime UTR variant
orthologous variants: 32350976-C-T

49366130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: missense variant
orthologous variants: 32350941-C-G

49366183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: missense variant
orthologous variants: 32350888-G-T

http://identifiers.org/hco/10/GRCh38#49366245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32350826-C-A

http://identifiers.org/hco/10/GRCh38#49366267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32350804-C-A

49366267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: missense variant
orthologous variants: 32350804-C-T

49366318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: missense variant
orthologous variants: 32350753-C-G

49366392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32350679-A-G

49366400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32350671-C-T

49366431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32350641-T-A

49366431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32350641-T-C

http://identifiers.org/hco/10/GRCh38#49366463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32350616-C-A

49366477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32350604-G-T

49366489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32350592-C-T

49366574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32350507-A-T

49366707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32350387-G-A

49366744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32350350-C-T

49366965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32350138-A-G

49367050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32350063-T-C

49367621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron_variant, undefined
orthologous variants: 32349843-A-G

49367903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron_variant, undefined
orthologous variants: 32349577-G-A

49367944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32349527-C-T

49367950-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32349521-G-C

49368103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32349349-A-G

49368148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32349300-C-T

49368331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32349206-A-T

49368510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32349026-G-A

49368510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32349026-G-C

49369159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32348266-C-T

49369305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32348150-T-A

49369315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32348141-C-T

49369363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32348092-G-A

49369363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32348092-G-C

49369405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32348064-A-T

49369475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32347999-T-A

49370738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32346611-G-T

49370912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32346432-C-G

49370925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32346419-G-A

49370950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32346393-G-A

49371024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32346332-G-A

49371161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32346196-T-G

49371303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32346037-T-G

49371687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32345642-G-C

49371757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32345590-A-G

http://identifiers.org/hco/10/GRCh38#49372486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32345063-A-C

49372793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32344814-A-G

49373840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32343736-T-C

49373853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32343723-A-G

49373859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32343717-C-T

49373866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32343710-A-G

49374118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32343446-C-G

http://identifiers.org/hco/10/GRCh38#49374241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32343334-A-C

49375448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32342577-T-C

49375452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32342573-T-C

49375459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32342566-T-C

49375524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32342503-A-G

49375820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32342228-C-T

49375929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32342149-T-A

49376048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32342031-G-A

49376326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32341441-G-A

49376429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32341350-A-G

49376429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32341350-A-T

49376718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32341106-T-C

49377467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32340431-T-C

49377651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32340262-G-T

49377712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32340105-A-G

49377758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32340068-C-T

49377792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32340037-G-A

http://identifiers.org/hco/10/GRCh38#49378770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32337689-A-C

49378770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32337689-A-T

49379423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32337044-T-A

49379423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32337044-T-C

49379590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32336697-C-T

49379758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32336565-A-G

49379867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron_variant, undefined
orthologous variants: 32336489-G-A

http://identifiers.org/hco/10/GRCh38#49379914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32336449-C-A

49379918-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32336445-C-G

49380187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32336214-T-C

49380374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32336037-A-T

49380569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32335851-A-G

49380710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32335504-A-G

49380792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32335423-G-A

49380902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32335336-C-T

49380903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32335335-A-G

49381081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32335172-G-T

49381131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32335114-C-T

49381230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32335041-C-T

http://identifiers.org/hco/10/GRCh38#49381233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32335038-C-A

49381646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32334771-G-A

49381815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32334650-C-T

49381886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32334587-G-A

49382022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32334478-G-A

49382029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32334471-T-C

49382319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32334244-T-A

49382338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32334228-A-G

49382338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32334228-A-T

http://identifiers.org/hco/10/GRCh38#49382357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32334195-C-A

49382549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32333996-T-C

49382556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32333989-C-T

49382575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32333970-G-A

http://identifiers.org/hco/10/GRCh38#49382879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32333842-A-C

49383125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32333691-T-C

49383176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32333646-C-T

49383177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32333645-C-T

49383289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32333547-A-G

49383296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32333540-C-T

49383402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32333431-G-A

49383412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32333421-A-G

49383436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32333398-G-A

49383437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32333397-G-A

49383470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32333324-T-C

http://identifiers.org/hco/10/GRCh38#49383882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32332919-A-C

49383895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32332901-T-G

49384073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32332716-C-T

49384299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32332334-A-G

49384316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32332314-C-T

http://identifiers.org/hco/10/GRCh38#49384390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32332216-C-A

49384390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32332216-C-T

49384516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32332087-C-T

49384612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32331995-A-G

49384714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32331905-G-T

49384756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32331864-C-T

http://identifiers.org/hco/10/GRCh38#49384819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32331798-C-A

49385237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32331492-C-T

http://identifiers.org/hco/10/GRCh38#49385672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32331178-C-A

49385672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32331178-C-T

49386019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32330828-C-T

49386020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32330827-A-G

49386142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32330694-G-A

http://identifiers.org/hco/10/GRCh38#49386447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32330436-C-A

49386447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32330436-C-G

49386447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32330436-C-T

http://identifiers.org/hco/10/GRCh38#49386457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32330429-C-A

49386457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32330429-C-G

49386457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32330429-C-T

49386464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32330422-G-A

49386464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32330422-G-C

49386464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32330422-G-T

49386470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32330416-A-G

http://identifiers.org/hco/10/GRCh38#49386564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32330322-C-A

49386566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: synonymous variant
orthologous variants: 32330320-T-C

49386566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: synonymous variant
orthologous variants: 32330320-T-G

49386637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32330251-G-T

http://identifiers.org/hco/10/GRCh38#49386694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32330195-C-A

49386694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: synonymous variant
orthologous variants: 32330195-C-T

http://identifiers.org/hco/10/GRCh38#49386925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32329960-C-A

49386925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32329960-C-G

http://identifiers.org/hco/10/GRCh38#49386932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32329953-C-A

49386932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32329953-C-T

49386934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32329951-G-A

http://identifiers.org/hco/10/GRCh38#49386969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32329921-A-C

49387008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32329889-G-A

49387008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32329889-G-T

http://identifiers.org/hco/10/GRCh38#49387052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#32329849-A-C

49387075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32329826-C-T

49387351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32329589-T-C

49387740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32329552-T-C

49388257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32329099-C-G

49388799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32328551-G-A

49389691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32327699-G-C

49389729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32327661-C-T

49390350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32327059-G-A

49390350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32327059-G-T

49390620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32326411-T-C

49391050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32326056-T-A

49391168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: missense variant
orthologous variants: 32325944-T-C

49391252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: missense variant
orthologous variants: 32325860-G-A

49391262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: undefined
orthologous variants: 32325850-C-T

49391689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32325364-T-C

49391781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32325296-T-C

49391787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32325290-A-G

http://identifiers.org/hco/10/GRCh38#49391931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32325157-C-A

49391931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32325157-C-T

http://identifiers.org/hco/10/GRCh38#49391946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32325143-C-A

49391982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32325107-T-C

49392016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32325072-A-T

49392576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32324525-A-T

49392762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32324376-A-G

49393163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32324006-C-G

49393163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32324006-C-T

49393219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32323950-T-A

49393292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32323870-G-A

49393292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32323870-G-T

http://identifiers.org/hco/10/GRCh38#49393398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32323783-C-A

49393895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32323334-C-T

http://identifiers.org/hco/10/GRCh38#49393922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32323288-A-C

http://identifiers.org/hco/10/GRCh38#49394126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32323111-C-A

49394612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32322784-A-G

49394612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32322784-A-T

49394773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32322622-G-A

49394776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32322619-G-A

49394778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32322617-G-A

49394905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32322484-G-T

49395146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron_variant, undefined
orthologous variants: 32322264-G-C

49395272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32322152-A-G

http://identifiers.org/hco/10/GRCh38#49395490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32321936-A-C

http://identifiers.org/hco/10/GRCh38#49395504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32321918-C-A

49395504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 5 prime UTR variant
orthologous variants: 32321918-C-G

49395504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: 5 prime UTR variant
orthologous variants: 32321918-C-T

http://identifiers.org/hco/10/GRCh38#49395579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32321855-C-A

49395579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32321855-C-T

http://identifiers.org/hco/10/GRCh38#49395667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#32321756-C-A

49395861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32321574-T-A

49395908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21536
most severe consequence: intron variant
orthologous variants: 32321528-G-A