132271986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445768-G-A

132271986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445768-G-T

132272012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445794-G-A

132272012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445794-G-T

http://identifiers.org/hco/6/GRCh38#132272047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445812-C-A

132272075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445840-T-C

132272081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445846-G-T

132272082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445847-A-G

132272084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445849-A-G

132272091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445856-G-T

132272099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445864-T-C

132272126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445891-G-A

132272126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445891-G-T

132272141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445906-T-C

http://identifiers.org/hco/6/GRCh38#132272143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445908-C-A

132272143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445908-C-T

132272145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445910-T-C

132272153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445918-G-A

132272153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445918-G-T

132272156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445921-T-A

132272156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445921-T-C

132272166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445931-G-T

132272173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445938-G-A

132272173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445938-G-T

132272177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445942-A-G

http://identifiers.org/hco/6/GRCh38#132272178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445943-C-A

132272178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445943-C-G

132272178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445943-C-T

http://identifiers.org/hco/6/GRCh38#132272189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445954-A-C

132272189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445954-A-G

132272191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445956-T-A

132272191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445956-T-C

132272195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445960-T-C

http://identifiers.org/hco/6/GRCh38#132272202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40445967-C-A

132272202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445967-C-T

132272213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445978-T-C

132272225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445990-G-T

132272231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40445996-T-C

http://identifiers.org/hco/6/GRCh38#132272237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446002-C-A

132272237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446002-C-G

132272237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446002-C-T

132272238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446003-A-G

132272245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446027-G-T

132272250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446032-T-C

132272251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446033-A-G

http://identifiers.org/hco/6/GRCh38#132272253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446035-C-A

132272253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446035-C-G

132272261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446043-T-G

http://identifiers.org/hco/6/GRCh38#132272271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446053-C-A

132272271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446053-C-T

http://identifiers.org/hco/6/GRCh38#132272277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446059-C-A

http://identifiers.org/hco/6/GRCh38#132272278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446060-C-A

132272279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446061-A-G

132272279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446061-A-T

132272281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446063-G-T

132272295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446077-C-T

132272298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446080-G-T

132272302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446084-G-A

132272302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446084-G-T

http://identifiers.org/hco/6/GRCh38#132272304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446086-C-A

132272304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446086-C-T

132272320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446102-G-C

132272320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446102-G-T

132272326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446108-G-C

132272346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446128-T-C

132272347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446129-G-C

132272347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446129-G-T

132272348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446130-G-A

132272348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446130-G-T

http://identifiers.org/hco/6/GRCh38#132272357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446139-C-A

132272357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446139-C-T

132272359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446141-G-A

132272359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446141-G-T

http://identifiers.org/hco/6/GRCh38#132272383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446165-C-A

132272383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446165-C-T

132272394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446176-A-G

132272400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446182-A-G

132272400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446182-A-T

132272405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446187-T-A

132272405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446187-T-C

132272406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446188-T-C

132272430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446212-T-A

132272430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446212-T-C

http://identifiers.org/hco/6/GRCh38#132272439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446221-C-A

132272439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446221-C-T

132272444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446227-G-A

132272444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446227-G-T

132272456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446239-T-A

132272456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446239-T-C

132272457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446240-G-A

132272457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446240-G-C

132272457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446240-G-T

132272465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446248-T-C

132272466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446249-G-A

132272466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446249-G-T

132272483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446266-T-C

132272510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446293-T-A

132272510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446293-T-C

132272532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446315-A-G

132272545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446328-A-G

132272545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446328-A-T

132272568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446351-T-A

132272568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446351-T-C

http://identifiers.org/hco/6/GRCh38#132272576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446359-C-A

132272576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446359-C-T

132272579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446362-G-A

132272579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446362-G-T

132272591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446374-G-A

132272591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446374-G-T

132272601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446384-G-T

132272607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446390-G-A

132272607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446390-G-C

132272607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446390-G-T

132272609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446392-T-A

132272609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446392-T-C

http://identifiers.org/hco/6/GRCh38#132272612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446395-A-C

132272612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446395-A-G

132272620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446403-A-G

http://identifiers.org/hco/6/GRCh38#132272624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446407-C-A

132272635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446418-T-C

132272636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446419-G-A

132272636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446419-G-T

http://identifiers.org/hco/6/GRCh38#132272637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446420-C-A

132272637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446420-C-T

132272639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446422-G-A

132272639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446422-G-T

132272641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446424-T-A

132272641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446424-T-C

132272648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446431-T-C

http://identifiers.org/hco/6/GRCh38#132272649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446432-C-A

132272649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446432-C-G

132272649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446432-C-T

http://identifiers.org/hco/6/GRCh38#132272654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446437-C-A

132272654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446437-C-G

132272654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446437-C-T

132272655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446438-T-A

132272655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446438-T-C

http://identifiers.org/hco/6/GRCh38#132272661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446444-C-A

132272661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446444-C-G

132272661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446444-C-T

132272663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446446-A-G

132272663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446446-A-T

http://identifiers.org/hco/6/GRCh38#132272673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446456-C-A

132272673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446456-C-T

http://identifiers.org/hco/6/GRCh38#132272676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446459-C-A

132272676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446459-C-T

132272695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446478-G-A

132272695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446478-G-C

132272695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446478-G-T

132272710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446493-A-G

http://identifiers.org/hco/6/GRCh38#132272742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446525-C-A

132272742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446525-C-T

http://identifiers.org/hco/6/GRCh38#132272750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446533-C-A

132272750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446533-C-T

132272763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446546-G-T

132272774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446557-A-G

http://identifiers.org/hco/6/GRCh38#132272802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446587-C-A

132272835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446620-G-A

132272835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446620-G-T

132272852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446637-G-A

132272890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446676-A-G

http://identifiers.org/hco/6/GRCh38#132272899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446685-C-A

132272899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446685-C-G

132272899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446685-C-T

132272900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446686-T-A

132272900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446686-T-C

132272904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446690-A-G

132272917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446703-G-A

132272917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446703-G-T

http://identifiers.org/hco/6/GRCh38#132272923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446709-A-C

132273022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446806-G-A

132273022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446806-G-C

132273022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446806-G-T

132273040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446824-T-A

132273040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446824-T-C

132273040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446824-T-G

132273052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446836-G-A

132273052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446836-G-C

132273052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446836-G-T

132273090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446874-T-A

132273090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446874-T-C

132273105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446889-G-A

132273105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446889-G-C

132273105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446889-G-T

132273137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446921-G-A

132273137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446921-G-T

132273146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446930-T-C

http://identifiers.org/hco/6/GRCh38#132273151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446937-A-C

132273159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446945-T-C

132273163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446949-A-G

132273182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446968-G-C

132273182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446968-G-T

132273185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446971-G-A

132273185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446971-G-T

132273192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446978-G-T

132273202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446988-G-T

132273210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446996-T-C

http://identifiers.org/hco/6/GRCh38#132273212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40446998-C-A

132273212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446998-C-T

132273213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40446999-T-C

http://identifiers.org/hco/6/GRCh38#132273214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447000-C-A

132273214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447000-C-T

132273216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447002-A-G

132273216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447002-A-T

132273237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447023-T-C

132273243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447029-A-G

132273244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447030-T-A

132273244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447030-T-C

132273246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447032-G-C

132273246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447032-G-T

132273247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447033-A-G

http://identifiers.org/hco/6/GRCh38#132273248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447034-C-A

132273248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447034-C-G

132273248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447034-C-T

132273255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447041-T-C

132273268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447055-G-A

132273268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447055-G-C

132273268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447055-G-T

132273272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447059-A-G

132273272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447059-A-T

132273276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447072-G-A

132273276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447072-G-T

132273279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447075-G-A

132273279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447075-G-C

132273279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447075-G-T

http://identifiers.org/hco/6/GRCh38#132273286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447082-C-A

132273286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447082-C-T

132273289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447085-G-A

132273289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447085-G-C

132273289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447085-G-T

http://identifiers.org/hco/6/GRCh38#132273298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#40447094-C-A

132273298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447094-C-G

132273298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447094-C-T

132273300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447096-G-A

132273300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447096-G-T

132273301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447097-A-G

132273301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37914
most severe consequence: non coding transcript exon variant
orthologous variants: 40447097-A-T