http://identifiers.org/hco/10/GRCh38#125576531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133120642-C-A

125576531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 133120642-C-T

http://identifiers.org/hco/10/GRCh38#125576545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133120656-C-A

125576578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 133120688-A-G

125578253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133125387-G-T

125578271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133125406-T-C

125578774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133125878-T-G

125578845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133125949-T-C

125580078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133126700-G-A

125580078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133126700-G-T

125580115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133126737-G-A

125580141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133126760-T-C

125580204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133126823-C-T

125580237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133126856-C-T

125580382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133126985-A-G

125580507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127111-G-A

125580681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127272-G-T

125580751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127317-C-G

125580827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127369-G-A

125580866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127382-G-A

125580941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127417-A-G

125580941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127417-A-T

125580951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127428-C-G

125581104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127539-C-G

125581213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127651-G-A

http://identifiers.org/hco/10/GRCh38#125582645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133128224-C-A

125582645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133128224-C-T

125582930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127943-C-T

125582937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127936-A-G

125582937-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127936-A-T

125583039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133127833-C-T

125584355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133138008-G-A

125590930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133138185-C-T

125591020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133138273-C-T

125591356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133138844-C-G

125591385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133138873-T-C

125591483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133138973-G-A

125591491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133138981-G-A

125591624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133139115-A-G

125591639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133139130-T-C

125591785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133139276-C-T

125592182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133139672-T-C

125592206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133139696-G-A

http://identifiers.org/hco/10/GRCh38#125592213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133139703-A-C

125592232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133139720-G-A

125592274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133139762-C-G

http://identifiers.org/hco/10/GRCh38#125592289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133139777-C-A

125592289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133139777-C-G

125592289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133139777-C-T

125592290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133139778-G-A

125592290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133139778-G-T

125592358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133139831-C-T

125592367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133139840-A-G

125598658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133143571-G-A

125598773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133143679-A-G

125598947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133143843-T-C

http://identifiers.org/hco/10/GRCh38#125599032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133143912-C-A

125599199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133144075-T-C

125599233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133144102-A-G

125599305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133144174-T-C

125599356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133144224-C-T

125600552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133144659-A-G

http://identifiers.org/hco/10/GRCh38#125600671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133144774-C-A

125600698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133144801-A-G

125600718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133144821-C-T

125600828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133144922-C-G

125600880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133144971-C-T

125600956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133145045-G-C

125601355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133145775-G-A

125601381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133145801-T-C

125601591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133146002-A-T

http://identifiers.org/hco/10/GRCh38#125601785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133146093-C-A

125601930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133146259-G-T

http://identifiers.org/hco/10/GRCh38#125601934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133146263-C-A

125601987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133146331-C-T

125601990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133146334-C-T

125602050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133146388-G-A

125602050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133146388-G-T

125602290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133146586-A-G

125602292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133146588-G-A

http://identifiers.org/hco/10/GRCh38#125602472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133146927-C-A

125602473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133146928-C-T

http://identifiers.org/hco/10/GRCh38#125602550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133147005-C-A

125602550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133147005-C-T

125602690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133147121-T-C

125606593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133150349-G-C

125606618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133150373-G-A

125606716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133150471-G-A

125606876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133150631-G-A

125606950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133150704-C-T

125606960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133150714-G-A

125606960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133150714-G-T

125607226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133150982-C-T

125607300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133151059-C-T

125607454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133151204-A-G

125607465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133151215-G-A

125607465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133151215-G-C

http://identifiers.org/hco/10/GRCh38#125607580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133151334-C-A

125607753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133151506-A-G

125607787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133151537-C-G

125607980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133152062-G-C

125607980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133152062-G-T

125608111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133152210-G-A

125608227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133152315-T-C

125610527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133155128-G-A

125610850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133155550-A-G

http://identifiers.org/hco/10/GRCh38#125610873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133155570-C-A

125610874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133155571-A-G

125611140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133155845-G-A

125611256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133155952-C-T

125611264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133155960-G-A

125611648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133156300-T-C

125612514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133157067-C-T

125612519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133157072-G-A

125612648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133157288-T-C

125612649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133157289-G-A

125613088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133157746-T-C

125613098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133157757-T-C

125613099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133157758-C-T

125613148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133157804-G-A

125613163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133157819-T-G

125620194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133159437-T-C

125620220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133159466-A-G

125620327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133159569-G-A

125620327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133159569-G-C

125620327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133159569-G-T

125620479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133159712-G-A

125620515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133159760-G-A

125620638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133159950-C-T

125620651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133159962-G-C

125620766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133160070-T-C

125620898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133160199-G-C

125620898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133160199-G-T

125621041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133160341-T-C

125621237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133160451-T-C

125623630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133160867-C-T

125623677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133160909-G-A

125623677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133160909-G-T

125624137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133162580-A-G

125624230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133162679-A-G

125624279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133162716-G-A

125624487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133162832-G-C

125624594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133162932-T-G

http://identifiers.org/hco/10/GRCh38#125624641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133162969-C-A

125624852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133163159-G-A

http://identifiers.org/hco/10/GRCh38#125624892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#133163198-A-C

125625282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133163565-T-G

125625400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133163669-G-A

125625403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133163672-A-G

125625412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133163681-A-G

125625461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133163723-G-A

125625461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133163723-G-C

125625732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133164428-A-G

125625744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133164440-C-T

125625938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133164616-G-T

125625975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133164648-A-T

125626090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133164788-C-T

125626091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133164789-A-T

http://identifiers.org/hco/10/GRCh38#125626177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133164878-C-A

125626177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133164878-C-T

125626186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133164887-C-G

http://identifiers.org/hco/10/GRCh38#125626275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133164970-C-A

125626542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133165169-T-C

125626898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133165518-G-A

125626898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133165518-G-C

125626942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133165596-A-G

125627182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133165884-T-C

125627224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133165948-C-T

125627587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133166318-C-T

125627693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133166411-T-C

125627740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133166454-T-A

125627740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133166454-T-C

125627756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133166471-A-G

125627826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133166537-G-A

125628375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133171543-G-T

125628917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133172436-T-C

125628918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133172437-G-C

125628996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133172503-G-A

125629205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133173062-A-T

125629252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133173178-T-A

125629252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133173178-T-C

http://identifiers.org/hco/10/GRCh38#125629316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133173240-A-C

125629547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133173474-T-G

125629553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133173480-G-A

125629553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133173480-G-C

125629553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133173480-G-T

125629700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133173625-G-A

125630102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133173916-G-A

125630190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133173987-A-G

125633327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133174633-A-G

125633328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133174634-C-T

125633491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133174788-A-G

125633568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133174859-A-G

125633683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, undefined
orthologous variants: 133174966-T-C

http://identifiers.org/hco/10/GRCh38#125633815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133175066-C-A

125633815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133175066-C-G

125633849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133175100-G-A

125634148-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133175347-T-A

125634148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133175347-T-C

125634355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133175539-G-A

125634788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133175966-T-C

125634841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133176027-G-T

125634903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133176087-T-C

125635122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133176284-G-C

125635309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133176885-T-C

http://identifiers.org/hco/10/GRCh38#125635583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133177114-C-A

125635583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133177114-C-T

125636573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133177377-T-G

125636586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133177390-A-T

125636698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133177482-C-T

125636892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133177673-A-G

125636947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133177730-C-G

125636971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133177754-G-A

125636971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133177754-G-T

125638694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133179073-G-A

http://identifiers.org/hco/10/GRCh38#125638830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133179195-C-A

125638830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133179195-C-T

http://identifiers.org/hco/10/GRCh38#125638854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133179214-C-A

125638859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133179219-T-G

125638891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133179252-C-G

125638931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133179292-T-A

125639425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133179771-G-T

125639586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133180758-A-G

125639586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133180758-A-T

125639592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133180764-T-A

125639592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133180764-T-G

125639595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133180767-G-A

125639630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133180790-A-G

125639894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133181191-G-A

125639900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133181197-G-A

http://identifiers.org/hco/10/GRCh38#125640071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133181350-A-C

125640071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 133181350-A-T

125640258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133181501-G-A

125640260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133181503-G-T

125640438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133181667-A-T

125640748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133181976-G-T

125640822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133182049-T-C

125640856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133182083-T-C

125641058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133182269-C-T

125641341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133183537-G-T

125641656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133183870-G-C

125641663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133183877-G-A

125642033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133184168-G-A

125642420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133184430-G-A

125642471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133184474-C-T

125642472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133184475-G-A

125642558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133184566-T-C

125642581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133184587-T-C

125642657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133184664-G-A

125642909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133184782-G-T

125643126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133184952-A-T

125643189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133185012-T-C

125643201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133185024-G-T

125655548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133188701-C-T

125655585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133188737-G-T

http://identifiers.org/hco/10/GRCh38#125655683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133188806-C-A

125655930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 133189040-G-A

125655976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, missense_variant
orthologous variants: 133189086-T-C

125655976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, missense_variant
orthologous variants: 133189086-T-G

125656074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 133189184-G-A

125656074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, stop_gained
orthologous variants: 133189184-G-C

http://identifiers.org/hco/10/GRCh38#125656097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133189207-A-C

125656194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 133189304-G-A

125656194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 133189304-G-T

125656239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133189347-T-C

http://identifiers.org/hco/10/GRCh38#125656240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133189348-C-A

125656240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133189348-C-T

125656731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133189498-C-G

125656731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133189498-C-T

125657155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133189837-G-A

125657214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133189950-T-C

125657214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133189950-T-G

125657350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133190308-G-A

125657434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133190427-C-T

125657435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133190428-G-A

125657435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133190428-G-T

125657454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133190440-T-A

125657455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133190441-C-T

125657456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133190442-G-A

http://identifiers.org/hco/10/GRCh38#125657467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133190453-A-C

125657472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133190459-C-T

125657693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133190712-C-G

http://identifiers.org/hco/10/GRCh38#125657788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133190805-C-A

125657831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133190847-G-A

125657905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133190948-A-G

125658001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133191116-G-A

125658045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133191235-T-A

125658130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133191340-G-A

125658130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133191340-G-C

125658470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133192176-G-A

125658520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133192220-G-T

125658618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133192304-C-T

125658965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133192889-A-T

125659039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133192960-A-G

http://identifiers.org/hco/10/GRCh38#125659046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133192965-A-C

125659136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133193063-T-C

125659225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133193209-A-G

http://identifiers.org/hco/10/GRCh38#125659273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133193259-C-A

125660851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133195871-G-A

125660860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133195886-A-G

http://identifiers.org/hco/10/GRCh38#125660914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133195940-C-A

125660914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133195940-C-T

125660938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133195969-C-T

125660947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133195978-T-C

125660960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133195991-G-T

125661033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: synonymous variant
orthologous variants: 133196147-G-A

125661033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: missense variant
orthologous variants: 133196147-G-C

125661070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: missense variant
orthologous variants: 133196184-A-T

125661129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133196241-G-A

125661129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133196241-G-T

125661178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133196291-G-A

125661235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133196349-G-A

125661235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133196349-G-C

125661235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133196349-G-T

125661386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133196486-C-G

http://identifiers.org/hco/10/GRCh38#125661501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133196625-C-A

http://identifiers.org/hco/10/GRCh38#125661517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133196677-C-A

125661519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133196679-T-C

125661632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133196758-G-A

125661692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133196817-G-T

125661780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133196878-G-T

125661825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133196914-T-C

125661949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: missense variant
orthologous variants: 133197036-G-A

http://identifiers.org/hco/10/GRCh38#125661994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133197081-C-A

125661994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133197081-C-T

125662031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133197118-C-G

http://identifiers.org/hco/10/GRCh38#125662069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133197154-C-A

125662104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133197189-A-G

http://identifiers.org/hco/10/GRCh38#125680166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133200059-C-A

125680166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133200059-C-T

125680167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133200060-G-A

125680170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133200063-T-C

125680227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133200115-G-A

125680470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133200357-G-A

125680614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133200504-T-A

125680910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133200810-C-T

125680961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133200858-G-A

http://identifiers.org/hco/10/GRCh38#125680988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133200878-A-C

125680988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133200878-A-G

125681304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133201167-G-A

125681324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133201256-G-C

http://identifiers.org/hco/10/GRCh38#125681500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#133201462-C-A

125681734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133201751-A-G

125682134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133202505-G-A

125682210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133202570-G-T

125682381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133202727-T-C

125682839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133203596-T-C

125682852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: intron variant
orthologous variants: 133203610-A-G

125682948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: synonymous variant
orthologous variants: 133203706-A-G

125683052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 5 prime UTR variant
orthologous variants: 133203791-T-C

125683084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 5 prime UTR variant
orthologous variants: 133203809-C-T

125683089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 5 prime UTR variant
orthologous variants: 133203814-C-T

125683102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31653
most severe consequence: 5 prime UTR variant
orthologous variants: 133203827-C-T