93478744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 15456300-C-T

93478827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: 3 prime UTR variant
orthologous variants: 15456232-A-T

http://identifiers.org/hco/11/GRCh38#93478831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15456228-C-A

93478838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: 3 prime UTR variant
orthologous variants: 15456221-C-T

93478936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 15456110-A-G

93478987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 15456100-G-A

93478987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 15456100-G-T

93479023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: missense variant
orthologous variants: 15456080-G-C

93479023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: missense variant
orthologous variants: 15456080-G-T

93479038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 15456065-A-G

93479080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 15456023-G-A

93479211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15455892-G-A

http://identifiers.org/hco/11/GRCh38#93479282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15455820-C-A

93479310-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15455786-T-A

93479310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15455786-T-C

93479310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15455786-T-G

93479924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15454866-C-T

93480405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15454429-G-A

93480482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15454387-T-A

93480665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15454220-T-C

93480759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15454113-G-A

93480809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15454035-G-A

93481077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15453669-C-T

93481326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15453486-C-T

93481340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15453472-G-T

93481357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15453454-C-T

93481643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15453231-T-C

93481655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15453216-C-T

http://identifiers.org/hco/11/GRCh38#93481661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15453210-C-A

93481798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15453119-G-A

93482080-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15452887-G-C

http://identifiers.org/hco/11/GRCh38#93482210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15452776-A-C

93482332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15452654-C-T

93482801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15451503-C-T

93482980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15451329-A-G

93482983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15451326-G-A

93483076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15451226-G-A

93483076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15451226-G-C

93483280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15450937-G-A

93483406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15450838-G-A

93483424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15450820-G-A

93483627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15450596-G-A

93483627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15450596-G-C

93483882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15450382-G-A

93483882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15450382-G-C

93483901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15450361-C-T

93483916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15450345-C-T

93484102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15450043-C-T

93484136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15450011-C-T

93484149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15449998-G-T

93484246-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15449921-T-A

93484506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15449617-C-G

93484896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15449028-T-G

93485764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15448153-T-C

93485776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15448106-A-G

93485832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15448054-C-T

93486318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15447649-A-G

93486645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15447291-C-T

93486776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15447191-C-T

93487237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron_variant, undefined
orthologous variants: 15447040-T-C

93487324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron_variant, undefined
orthologous variants: 15446955-C-T

93487360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron_variant, undefined
orthologous variants: 15446919-A-G

93487472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron_variant, undefined
orthologous variants: 15446828-C-T

93487628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15446709-A-G

93487694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15446645-T-C

93487928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15446442-C-T

93488249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15446220-G-A

93488273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15446196-C-T

93488466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15445583-C-T

93488520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15445544-C-T

http://identifiers.org/hco/11/GRCh38#93488718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15445372-C-A

http://identifiers.org/hco/11/GRCh38#93488746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15445340-C-A

93488843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15445250-C-G

93488843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15445250-C-T

93488981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15445136-T-A

93488981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15445136-T-C

93488982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15445135-G-A

93489204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15445018-T-C

93489333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15444888-A-G

93489507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15444753-C-G

93489971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15444542-G-T

93490842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15444344-C-T

93490905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15444283-A-T

93491071-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15444133-T-A

93491247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15443957-G-C

93491277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15443935-G-C

http://identifiers.org/hco/11/GRCh38#93491350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15443861-A-C

93491380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15443830-T-C

http://identifiers.org/hco/11/GRCh38#93491405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15443805-C-A

93491463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15443753-C-T

http://identifiers.org/hco/11/GRCh38#93491864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15443380-C-A

93491989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15443257-A-G

93492087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15443147-A-G

93492120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15443117-A-G

93492138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15443099-A-G

http://identifiers.org/hco/11/GRCh38#93492233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15442986-C-A

http://identifiers.org/hco/11/GRCh38#93492371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15442868-A-C

93492549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15442736-G-T

93492569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15442729-G-A

93492767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15442572-T-C

93492797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15442542-C-T

93492842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15442498-T-C

93492842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15442498-T-G

93493216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15442158-G-A

http://identifiers.org/hco/11/GRCh38#93493381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15442057-C-A

93493381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15442057-C-G

93493381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15442057-C-T

93493385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15442053-C-T

93493387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15442051-C-G

93493746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15441809-C-T

93493788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron_variant, undefined
orthologous variants: 15441772-T-C

93493849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15441735-C-T

93493857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15441727-C-G

93493857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15441727-C-T

93493960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15441608-A-G

93494031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15441524-T-C

93494059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15441497-G-C

93494112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15441446-T-C

93494261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15441305-T-C

93495460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15439884-A-G

93495728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15439642-A-T

93495729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15439641-C-T

93495769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15439601-T-C

93495769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15439601-T-G

93496023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15439414-G-A

93496081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15439391-G-A

93496154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15439322-T-C

93496369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15439138-T-G

http://identifiers.org/hco/11/GRCh38#93496672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15438889-C-A

93496851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15438325-C-T

93497108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15438089-T-G

93497624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15437608-G-A

93497705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15437545-A-G

93497779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15437475-G-T

93497849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15437404-G-C

93499235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15437027-T-C

http://identifiers.org/hco/11/GRCh38#93499431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15436853-C-A

93499682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15436667-G-A

93499746-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15436604-T-A

93499752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15436599-T-A

93499752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15436599-T-C

93499827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15436525-G-A

93499827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15436525-G-C

93499833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15436519-G-A

93499833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15436519-G-C

93499993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15436392-G-A

93500536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15436051-T-G

93500954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15435663-A-T

http://identifiers.org/hco/11/GRCh38#93501143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15435494-C-A

93501360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15435290-C-T

93501447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15435232-T-C

93501638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15435099-G-A

93501831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15434998-C-T

93502072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15434804-C-T

93502146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15434771-A-G

93502179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15434746-C-T

93502382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15434582-A-G

93502481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15434509-G-C

93502511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15434482-G-A

http://identifiers.org/hco/11/GRCh38#93502633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15434347-A-C

93502933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15434004-A-G

93502935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15434002-A-G

93502971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15433926-G-A

93503642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15433480-C-T

http://identifiers.org/hco/11/GRCh38#93503708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15433442-C-A

93503749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15433419-T-G

93503755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15433413-C-T

93503873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15433306-A-G

93503890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15433289-C-T

93503892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15433287-A-G

93503976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15433218-G-A

93503976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15433218-G-C

93504088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15433115-C-G

93508207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15430963-G-A

93508434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15430750-T-G

93508637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15430554-T-C

93508797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15430062-G-C

93508863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15429982-C-T

93510227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15429649-G-A

http://identifiers.org/hco/11/GRCh38#93514629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15427737-A-C

93514629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15427737-A-G

93514640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15427726-T-A

93514897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15427496-C-T

93515008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15427407-C-T

93515089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15427326-C-G

93515169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15427253-T-C

93519061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15424832-T-C

93519100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15424800-A-T

93519131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15424772-C-T

93519313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15424619-A-G

http://identifiers.org/hco/11/GRCh38#93519447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15424485-A-C

93519460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15424472-C-T

93519585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15424359-T-C

93519585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15424359-T-G

93519653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15424300-G-C

93519851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15424166-C-T

93519938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15424074-T-C

93520082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15423928-C-T

http://identifiers.org/hco/11/GRCh38#93520105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15423905-A-C

93520499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422791-G-A

93520536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422755-T-A

93520536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422755-T-C

93520700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422586-C-G

93520756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422534-G-A

93520830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422479-A-G

93520830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422479-A-T

93520845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422465-C-G

93520848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422462-C-T

93520854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422455-A-G

93520855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422454-C-T

93520884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422423-A-G

93521000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422306-T-C

93521004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422302-T-C

93521240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422096-A-G

93521330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15422030-A-G

93521458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15421908-T-C

93521650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15421382-C-T

93522946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15421007-G-C

93523097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15420873-G-C

93523204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15420790-A-G

http://identifiers.org/hco/11/GRCh38#93523231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15420770-C-A

http://identifiers.org/hco/11/GRCh38#93523307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15420707-C-A

93523307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15420707-C-T

http://identifiers.org/hco/11/GRCh38#93524247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15420030-A-C

93524331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15419957-G-A

93524403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15419901-C-T

93524594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15419586-T-C

93524694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15419486-C-T

http://identifiers.org/hco/11/GRCh38#93524760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15419420-C-A

93524772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15419408-T-C

93524821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15419356-C-G

93525302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15419019-T-C

93525532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15418784-C-T

93525801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15418505-G-C

93525822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15418480-C-G

http://identifiers.org/hco/11/GRCh38#93526218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15418120-C-A

93526218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15418120-C-T

93526244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15417976-C-T

http://identifiers.org/hco/11/GRCh38#93526266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15417956-C-A

93526266-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15417956-C-G

93526266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15417956-C-T

93526297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron_variant, undefined
orthologous variants: 15417949-T-A

93526354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15417889-C-T

93526408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15417824-A-G

93526529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15417676-T-C

93526709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron_variant, undefined
orthologous variants: 15417546-G-A

93526954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15417327-C-T

http://identifiers.org/hco/11/GRCh38#93527121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15417214-C-A

93527131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15417205-G-A

93527207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15417132-G-A

93527843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15416544-T-C

93528243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15416149-G-C

93528530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15415916-T-C

93528592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15415869-T-G

93528660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15415819-C-T

93528685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15415789-G-A

93529047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15415683-G-A

93529246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15415565-T-G

93529299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15415540-C-G

93529443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15415415-A-G

93529660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15415257-T-G

93529798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15415157-C-T

93529807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15415149-G-A

93529885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15415097-T-C

93530225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron_variant, undefined
orthologous variants: 15414801-G-A

http://identifiers.org/hco/11/GRCh38#93530430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#15414631-A-C

http://identifiers.org/hco/11/GRCh38#93530443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#15414615-A-C

http://identifiers.org/hco/11/GRCh38#93534351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15412378-C-A

93534353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15412376-C-T

93534377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15412352-G-T

93534430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15412307-G-T

93534431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15412306-T-G

93534516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15412225-C-G

93534588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15412131-C-T

93534728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15411990-G-A

93534774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15411959-G-A

93534966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15411795-C-G

93535127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15411678-C-T

93535164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15411642-T-C

93535204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15411602-C-T

93536282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15411266-A-G

93536313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15411235-A-G

93536339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15411209-T-C

93536383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15411194-T-C

http://identifiers.org/hco/11/GRCh38#93536580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15410979-A-C

93536581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15410978-G-A

93536664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15410892-T-C

93536760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15410806-C-T

93536820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15410753-C-T

93536872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15410710-A-G

93536893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15410689-C-T

93536928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15410660-T-C

http://identifiers.org/hco/11/GRCh38#93537091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15410533-C-A

93537123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15410524-G-A

93537357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15410297-A-G

93537372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15410282-G-A

93537473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15410186-T-G

http://identifiers.org/hco/11/GRCh38#93537574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15410079-C-A

93537574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15410079-C-G

93537574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15410079-C-T

93537648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15409980-C-T

93537811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15409833-A-G

http://identifiers.org/hco/11/GRCh38#93537935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15409726-C-A

http://identifiers.org/hco/11/GRCh38#93537945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15409716-C-A

93537945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15409716-C-T

93537950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15409707-T-C

93537952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15409705-T-C

http://identifiers.org/hco/11/GRCh38#93538035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15409640-C-A

93538035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15409640-C-T

93538376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15409402-C-T

http://identifiers.org/hco/11/GRCh38#93538495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15409279-C-A

93538495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15409279-C-T

93538651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15409149-T-C

93538723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15409085-C-T

93538818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15408995-C-T

93538974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15408838-C-T

93539157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15408589-G-T

93539229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15408499-A-G

93539557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15408231-C-T

http://identifiers.org/hco/11/GRCh38#93539708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15408087-A-C

93539753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15408043-G-C

93539753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15408043-G-T

93539779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15408018-G-T

93539901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15407907-C-T

93539975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15407866-A-G

93540078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15407769-C-G

93540144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15407702-G-T

93540171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15407675-A-G

93540301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15407546-G-A

http://identifiers.org/hco/11/GRCh38#93540403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15407468-C-A

93540403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15407468-C-T

93540764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15407144-T-A

93540856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15407057-G-T

93540958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15407028-A-T

http://identifiers.org/hco/11/GRCh38#93541322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15406445-A-C

93541663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15406161-C-G

93541861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15405977-G-T

93542013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron_variant, undefined
orthologous variants: 15405838-G-T

93542077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15405773-T-A

93542131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron_variant, undefined
orthologous variants: 15405742-C-T

93542209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron_variant, undefined
orthologous variants: 15405666-T-C

93542868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15405139-C-T

http://identifiers.org/hco/11/GRCh38#93543187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15404964-C-A

93544910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24810
most severe consequence: intron variant
orthologous variants: 15403078-C-G