87085506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122144116-G-A

87085560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122144167-T-C

87085588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122144189-A-G

87085601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122144203-T-G

87085620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122144226-A-G

87085909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122144509-T-C

87086000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122144598-G-A

87086296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122144769-A-G

87086330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122144803-C-G

87086500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122144915-A-G

http://identifiers.org/hco/16/GRCh38#87086872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122145231-A-C

87086985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145349-T-C

87087055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145424-G-T

87099000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145872-C-T

87099037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145905-G-C

87099044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122145912-G-A

87099235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122146097-A-T

87099363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122146202-G-A

87099363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122146202-G-C

87102086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148115-T-C

87102128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148157-C-T

87102233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148252-A-G

87102284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148303-C-T

87102557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122148565-G-C

http://identifiers.org/hco/16/GRCh38#87107122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122150593-C-A

87107327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122150812-T-A

87107327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122150812-T-C

87107449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122150926-C-T

87107580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122151020-T-G

87107587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122151027-C-T

87107597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122151037-T-C

87114554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122152703-G-C

87114567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122152714-A-G

87127061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122158316-T-C

87127173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122158424-C-T

87127442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122158620-G-A

87127491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122158666-C-G

87131380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122159202-G-C

87131398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122159220-C-G

87131489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122159294-C-T

87131596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122159399-C-T

87131613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122159416-A-T

87132512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122160112-C-T

87132551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122160150-G-A

http://identifiers.org/hco/16/GRCh38#87132627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122160228-C-A

87132627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122160228-C-T

87132712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122160319-T-G

87132746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122160356-C-T

87132825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 122160438-C-T

87133006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122160627-G-T

87133043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122160663-G-A

87133043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122160663-G-T

87133107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122160696-G-T

87133173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160750-G-A

87133190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160766-C-G

87133190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160766-C-T

http://identifiers.org/hco/16/GRCh38#87133224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122160803-C-A

87133224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160803-C-G

87133247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160814-G-T

87133253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160820-T-G

87133257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160824-T-C

87133317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160859-C-G

87133407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160912-G-A

http://identifiers.org/hco/16/GRCh38#87133462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122160975-C-A

87133462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160975-C-T

87133472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122160985-C-G

87135181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122162711-C-G

http://identifiers.org/hco/16/GRCh38#87135328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122162847-A-C

87135512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122162945-A-G

87135531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122162963-A-T

87135576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122163009-C-T

87135655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122163073-A-G

87140256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122163877-T-C

http://identifiers.org/hco/16/GRCh38#87140272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122163893-C-A

87140272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122163893-C-T

87140396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122163980-G-T

87140546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164116-G-A

87140584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164167-G-A

87140584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164167-G-T

http://identifiers.org/hco/16/GRCh38#87140673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122164226-C-A

87140673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164226-C-T

http://identifiers.org/hco/16/GRCh38#87140678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122164231-C-A

87140678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164231-C-T

87140679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164232-A-G

http://identifiers.org/hco/16/GRCh38#87140871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122164378-C-A

87140871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164378-C-T

87141026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164531-T-C

87141027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164532-G-A

87141027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164532-G-T

http://identifiers.org/hco/16/GRCh38#87141028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122164533-C-A

87141028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164533-C-T

87141076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164579-G-A

87141076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164579-G-C

87141076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122164579-G-T

87141292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122164771-C-G

http://identifiers.org/hco/16/GRCh38#87141642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122165107-C-A

87141642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122165107-C-T

87141666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122165129-C-T

87141724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122165188-C-T

87141788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122165250-G-A

http://identifiers.org/hco/16/GRCh38#87143771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122166160-A-C

87144080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122166433-C-T

87160472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122167422-C-T

87160778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122167129-A-T

87160852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122167086-G-C

87160888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122167053-T-C

87160947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122166994-T-C

87165663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122171384-T-A

87165893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122171580-A-T

87166043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122171707-A-T

87166370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122172037-C-T

87166556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122172197-T-C

87166560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122172201-C-T

87166561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122172202-G-A

87166561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122172202-G-T

http://identifiers.org/hco/16/GRCh38#87173409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122172909-C-A

87173560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173055-T-C

87173592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173089-C-T

http://identifiers.org/hco/16/GRCh38#87173637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122173131-A-C

87173678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173157-C-G

87173678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173157-C-T

87173816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173293-G-A

87173816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173293-G-C

87173816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173293-G-T

87173849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173317-C-G

87173916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173380-G-T

http://identifiers.org/hco/16/GRCh38#87173917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122173381-C-A

http://identifiers.org/hco/16/GRCh38#87173926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122173390-C-A

87173926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173390-C-T

http://identifiers.org/hco/16/GRCh38#87173931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122173395-C-A

87173931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173395-C-G

87173931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173395-C-T

87174159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173602-T-A

http://identifiers.org/hco/16/GRCh38#87174165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122173608-A-C

87174223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122173674-G-A

87177606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122176904-C-T

87177920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122177197-G-A

87177920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122177197-G-C

87178009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122177285-C-T

87178549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122177767-T-C

87178566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122177771-G-C

87178581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122177786-T-A

87178624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122177829-C-G

87178706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122177898-C-G

87178706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122177898-C-T

87178721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122177913-T-C

87178784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122177965-C-G

87178852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122177998-T-C

87178920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122178068-T-C

87179142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122178249-G-A

87179221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122178328-G-C

87179383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122178477-G-A

87179448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122178559-C-T

http://identifiers.org/hco/16/GRCh38#87182418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122180504-A-C

87182492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122180580-G-C

87185417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122181601-G-A

87185433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122181620-A-G

87185522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122181706-G-A

87185702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122181865-G-T

87185788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122181924-G-A

87186103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122182244-C-T

87186635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122182810-C-G

87186767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122182912-G-A

87187008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122183126-G-A

87192154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185299-T-C

87192193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185342-A-G

87192194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185343-T-C

http://identifiers.org/hco/16/GRCh38#87192197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122185346-A-C

87192212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185361-G-A

87192297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185436-G-A

87192729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185866-G-A

http://identifiers.org/hco/16/GRCh38#87192730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122185867-C-A

87192741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185877-G-A

87192741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185877-G-C

87192850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122185984-C-T

87196139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122187981-G-C

87196140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122187982-C-T

87196230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122188069-G-C

87211122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122191643-A-T

87211132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122191653-G-A

87211979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122192352-G-A

87211979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122192352-G-T

87212629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122193383-G-A

87215770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122194219-G-T

http://identifiers.org/hco/16/GRCh38#87215855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122194322-A-C

87215994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122194423-G-A

87215994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122194423-G-T

http://identifiers.org/hco/16/GRCh38#87216186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122194585-C-A

87216186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122194585-C-T

87216215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122194618-T-C

87216290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122194687-A-G

87216382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122194789-A-G

87216382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122194789-A-T

http://identifiers.org/hco/16/GRCh38#87216417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122194823-C-A

87216417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122194823-C-T

http://identifiers.org/hco/16/GRCh38#87216433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122194836-C-A

87216567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122194970-T-C

87216822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122195254-C-T

87216829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122195261-C-G

87216829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122195261-C-T

87217067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122195517-G-C

87217139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122195630-G-A

87217166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122195658-G-T

87217227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122195721-G-A

http://identifiers.org/hco/16/GRCh38#87222556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122200764-C-A

http://identifiers.org/hco/16/GRCh38#87222602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122200807-A-C

87222694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122200888-T-C

87222844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122201016-G-A

87223261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122201379-A-G

87223431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122201566-T-A

87223443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122201588-G-C

87223445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122201590-T-C

87223477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122201622-G-A

87226192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122203701-T-C

87226240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122203746-C-T

87226316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122203807-C-T

http://identifiers.org/hco/16/GRCh38#87227318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122204660-C-A

87227334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122204676-G-A

87227334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122204676-G-C

87227334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122204676-G-T

87227806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122205130-C-T

87227966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122205277-T-C

http://identifiers.org/hco/16/GRCh38#87227980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122205295-C-A

87228017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122205333-T-A

87228017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122205333-T-C

87228017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122205333-T-G

87233653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122210278-C-G

87234449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211122-T-C

87234528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211224-C-T

87234680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211379-G-A

87234680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211379-G-C

87234773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211472-G-C

87234790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211488-G-T

87235012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211677-A-G

87235012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211677-A-T

87235038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211704-A-G

87235133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211785-G-T

87235341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211949-T-C

87235390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122211979-C-T

87235590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122212353-G-A

http://identifiers.org/hco/16/GRCh38#87240522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#122212864-A-C

87240624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122212950-C-T

87240681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122212988-T-C

87240682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122212989-G-A

87240732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122213010-G-A

87240732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122213010-G-C

87240791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122213064-T-G

http://identifiers.org/hco/16/GRCh38#87240852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#122213105-C-A

87240852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122213105-C-T

87241038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122213252-T-A

87241038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122213252-T-C

87242946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122215730-G-C

http://identifiers.org/hco/16/GRCh38#87242964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122215748-C-A

87243159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122215919-C-T

87243175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122215937-G-A

87243417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122216105-C-T

87245175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122218131-G-C

87245175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122218131-G-T

87245232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122218182-C-G

87245252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122218202-G-A

87245258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122218208-G-A

87245481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122218446-G-A

87245557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122218510-T-C

87245557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122218510-T-G

87245604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122218545-C-T

http://identifiers.org/hco/16/GRCh38#87245624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122218563-A-C

87246261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122219109-G-A

87246261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122219109-G-C

87246382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122219187-G-A

87246382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122219187-G-C

87246770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122219493-T-C

http://identifiers.org/hco/16/GRCh38#87253992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122224995-C-A

87254023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225019-G-A

87254170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225126-G-C

http://identifiers.org/hco/16/GRCh38#87254225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122225174-A-C

http://identifiers.org/hco/16/GRCh38#87254277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122225226-A-C

87254277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225226-A-G

87254330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225279-C-T

87254336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225285-C-T

87254456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225404-G-A

87254584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225517-G-A

87254587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225520-G-A

87254610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225540-G-A

87254696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225597-G-A

87254735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225626-C-G

87254838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225709-A-T

http://identifiers.org/hco/16/GRCh38#87254916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122225760-A-C

87255030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225869-C-T

87255036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225875-T-C

87255095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122225924-T-C

87255178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122226014-G-A

87255274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122226104-G-T

87255445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122226247-G-A

87258053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122226944-T-C

87258053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122226944-T-G

87258071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122226962-G-A

87258273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122227164-G-C

87258388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122227298-C-T

87258394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122227304-C-T

87258400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122227310-A-G

87258431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122227345-T-C

87262311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122228059-T-A

87262452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122228200-T-C

http://identifiers.org/hco/16/GRCh38#87262503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122228255-C-A

87264812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122229507-T-C

87264903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122229612-C-T

http://identifiers.org/hco/16/GRCh38#87264908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122229617-C-A

87264908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122229617-C-G

87265109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122229810-G-A

http://identifiers.org/hco/16/GRCh38#87265365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122230093-C-A

87265365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122230093-C-T

87265513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122230231-A-T

87265547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122230264-G-A

87265556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122230271-G-T

87265702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122230416-G-A

87265741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122230455-T-A

87265786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122230478-G-C

87265817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122230516-C-T

87265898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122230573-C-T

87266010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122230669-T-C

87266293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122230932-T-C

http://identifiers.org/hco/16/GRCh38#87266473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122231090-C-A

87266473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231090-C-T

87266656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231171-G-A

87266892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231197-T-G

87266917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231219-G-A

87266967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231264-A-T

87267075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231369-T-G

87267138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231430-G-C

87267138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231430-G-T

87267145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231437-G-T

87267246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231527-G-A

87267246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231527-G-T

87267251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122231532-G-T

http://identifiers.org/hco/16/GRCh38#87267418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122231659-C-A

87267466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122231702-C-T

http://identifiers.org/hco/16/GRCh38#87267517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122231752-C-A

87267653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122231881-C-G

87267663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122231893-A-G

87267663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122231893-A-T

87267735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122231931-T-C

http://identifiers.org/hco/16/GRCh38#87267801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122231968-A-C

87267801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122231968-A-G

87267801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122231968-A-T

87267833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122231999-T-A

87267854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122232018-T-C

http://identifiers.org/hco/16/GRCh38#87267856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122232020-C-A

87267856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122232020-C-G

87267856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122232020-C-T

http://identifiers.org/hco/16/GRCh38#87271211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122233585-C-A

87271211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233585-C-T

87271426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233774-C-G

87271426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233774-C-T

87271477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233811-G-A

87271477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233811-G-C

87271489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233823-C-G

87271588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233881-C-T

87271684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233960-C-T

http://identifiers.org/hco/16/GRCh38#87271688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122233964-C-A

87271688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122233964-C-G

87271812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122234081-G-T

http://identifiers.org/hco/16/GRCh38#87271868-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122234124-A-C

87271924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122234173-A-G

87271935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122234190-A-G

87271935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122234190-A-T

87271939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122234194-T-C

87271940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122234195-G-A

http://identifiers.org/hco/16/GRCh38#87272101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122234343-C-A

87272198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122234431-G-C

87272198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122234431-G-T

87272200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122234433-C-T

87274521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122236506-G-A

http://identifiers.org/hco/16/GRCh38#87274563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122236550-C-A

87274580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122236567-C-T

87274718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122236625-T-C

87275278-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122237039-T-G

87275332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122237084-A-G

87275463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122237224-A-G

87275546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122237311-G-A

87275562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122237327-C-G

87275778-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122238481-G-C

87275896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122238602-A-G

87276047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122238738-T-G

87276160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122238839-G-A

87276307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122238956-G-A

87276597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122239268-C-T

87276771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122239424-G-A

87276771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122239424-G-T

87276779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122239432-C-T

87278612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240189-G-A

87278704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240292-T-A

87278823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240390-C-T

87278824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122240391-G-A

87295759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122251745-A-G

http://identifiers.org/hco/16/GRCh38#87295898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122251860-C-A

87295919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122251881-G-A

http://identifiers.org/hco/16/GRCh38#87296081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122252014-C-A

87296081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122252014-C-G

87302761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: non coding transcript exon variant
orthologous variants: 122257486-A-G

87302804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122257508-A-G

87302813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122257518-G-C

87302813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122257518-G-T

http://identifiers.org/hco/16/GRCh38#87302902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122257607-C-A

87302967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122257674-C-G

87303012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122257721-A-T

87303024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 122257735-G-A

87305720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 122258438-G-A

87305720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 122258438-G-C

87305720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 122258438-G-T

87305727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122258445-C-T

87305836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122258584-T-C

87305836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 122258584-T-G

87305847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122258595-G-A

87305847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 122258595-G-T

87305850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 122258598-C-T

87305901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 122258649-G-A

87305901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 122258649-G-T

http://identifiers.org/hco/16/GRCh38#87305911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#122258657-C-A

87305911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 122258657-C-T

http://identifiers.org/hco/16/GRCh38#87310222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122260386-C-A

87310222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122260386-C-T

http://identifiers.org/hco/16/GRCh38#87310223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122260387-C-A

87310345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122260482-G-A

http://identifiers.org/hco/16/GRCh38#87310375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122260552-C-A

87310375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122260552-C-T

87310386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122260563-A-G

87310474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122260623-G-A

87310474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122260623-G-C

87310474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122260623-G-T

87310493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122260642-C-T

87311034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122262102-G-A

87311034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122262102-G-T

87311074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122262114-T-C

87311092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122262122-T-A

87311092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122262122-T-C

http://identifiers.org/hco/16/GRCh38#87311094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122262124-C-A

87311094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122262124-C-G

87311094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122262124-C-T

http://identifiers.org/hco/16/GRCh38#87311096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122262126-C-A

87311096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122262126-C-T

http://identifiers.org/hco/16/GRCh38#87311106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122262135-A-C

http://identifiers.org/hco/16/GRCh38#87311118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122262147-A-C

87311118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122262147-A-G

http://identifiers.org/hco/16/GRCh38#87311252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122262264-C-A

87314894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122266534-C-G

87314905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122266545-G-A

87314905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122266545-G-C

87314905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122266545-G-T

87315088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: synonymous variant
orthologous variants: 122266738-A-G

http://identifiers.org/hco/16/GRCh38#87315113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122266763-A-C

87315145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122266793-A-G

87315145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122266793-A-T

http://identifiers.org/hco/16/GRCh38#87315191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122266840-A-C

http://identifiers.org/hco/16/GRCh38#87315229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122266875-C-A

87315229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122266875-C-T

87315232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122266878-G-A

87315232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122266878-G-T

http://identifiers.org/hco/16/GRCh38#87315295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122266912-C-A

87315295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122266912-C-T

87315319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122266936-G-A

87315519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267046-C-G

87315519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267046-C-T

87315524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267051-A-G

87315532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267059-C-G

http://identifiers.org/hco/16/GRCh38#87315579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122267106-C-A

87315601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267136-T-C

87315666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267194-G-C

http://identifiers.org/hco/16/GRCh38#87315838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122267334-C-A

http://identifiers.org/hco/16/GRCh38#87315846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122267349-C-A

87315846-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267349-C-G

87315846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267349-C-T

87315858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267361-G-A

87315858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267361-G-T

87315865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267368-A-G

87315865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267368-A-T

87315866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267369-G-A

87315866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267369-G-T

87315867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267370-G-A

87315867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267370-G-C

87315867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267370-G-T

http://identifiers.org/hco/16/GRCh38#87315879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122267372-C-A

87315879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267372-C-G

87315879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267372-C-T

http://identifiers.org/hco/16/GRCh38#87315887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122267380-C-A

87315887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267380-C-T

http://identifiers.org/hco/16/GRCh38#87315934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122267400-A-C

87315934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267400-A-G

87315934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267400-A-T

87315942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267408-T-A

87315942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267408-T-C

87315942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267408-T-G

87315954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267418-G-A

87315954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267418-G-C

87315954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267418-G-T

http://identifiers.org/hco/16/GRCh38#87315957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#122267421-C-A

87315957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267421-C-T

87315970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267434-G-T

87316330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267817-G-A

87316358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122267858-A-G

87316603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122268185-C-T

87316726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122268305-G-C

87316758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron variant
orthologous variants: 122268338-A-G

87316786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, undefined
orthologous variants: 122268358-G-A

87316864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, undefined
orthologous variants: 122268438-G-A

87316869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: intron_variant, undefined
orthologous variants: 122268443-A-G

http://identifiers.org/hco/16/GRCh38#87317404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#122268719-C-A

87317404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 122268719-C-T

http://identifiers.org/hco/16/GRCh38#87317406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#122268721-C-A

87317406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 122268721-C-G

http://identifiers.org/hco/16/GRCh38#87317412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#122268727-C-A

87317412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40033
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 122268727-C-T