27787762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125477802-C-T

27787909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125477944-C-T

27788062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125478040-A-T

http://identifiers.org/hco/16/GRCh38#27788240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125478174-C-A

27788240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125478174-C-T

27788328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125478254-A-G

27788328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125478254-A-T

http://identifiers.org/hco/16/GRCh38#27788330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125478256-C-A

27788667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125478537-C-T

http://identifiers.org/hco/16/GRCh38#27788712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125478587-C-A

27788712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125478587-C-G

27788742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125478608-T-C

27788781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125478659-C-T

27789835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125478950-T-G

27789973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479084-A-G

27789977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479088-C-T

http://identifiers.org/hco/16/GRCh38#27789981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125479092-A-C

27789981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479092-A-G

http://identifiers.org/hco/16/GRCh38#27789995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125479096-C-A

http://identifiers.org/hco/16/GRCh38#27790030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125479131-C-A

27790105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479226-G-T

27790209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479323-G-A

27790209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479323-G-T

27790292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479435-A-G

27790410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479535-G-T

27790528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479644-T-C

27790541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479657-A-G

27790600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479716-T-A

27790619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479734-G-A

27790619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479734-G-T

http://identifiers.org/hco/16/GRCh38#27790755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125479809-C-A

27790755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479809-C-T

27790830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479829-G-A

27790830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479829-G-T

27790848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479847-G-A

27790876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479855-T-C

http://identifiers.org/hco/16/GRCh38#27791001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125479976-C-A

http://identifiers.org/hco/16/GRCh38#27791003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125479978-A-C

27791003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479978-A-G

27791003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125479978-A-T

27791206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125480173-G-T

27791324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125480272-G-A

27791324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125480272-G-C

27791324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125480272-G-T

http://identifiers.org/hco/16/GRCh38#27791347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125480295-C-A

27791347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125480295-C-G

27791347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 3 prime UTR variant
orthologous variants: 125480295-C-T

http://identifiers.org/hco/16/GRCh38#27791373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125480316-C-A

27791373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: synonymous variant
orthologous variants: 125480316-C-T

27791415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: synonymous variant
orthologous variants: 125480358-T-C

27791415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: synonymous variant
orthologous variants: 125480358-T-G

http://identifiers.org/hco/16/GRCh38#27791421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125480364-C-A

27791421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: missense variant
orthologous variants: 125480364-C-G

27791421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: synonymous variant
orthologous variants: 125480364-C-T

http://identifiers.org/hco/16/GRCh38#27791539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125480461-C-A

27791539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125480461-C-T

http://identifiers.org/hco/16/GRCh38#27791540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125480462-C-A

27791540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125480462-C-G

27791540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125480462-C-T

27791661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125480517-T-A

27791661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125480517-T-C

27791669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125480525-C-T

http://identifiers.org/hco/16/GRCh38#27791799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125480599-C-A

27791799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125480599-C-G

27791799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125480599-C-T

http://identifiers.org/hco/16/GRCh38#27791808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125480608-C-A

27791810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125480610-T-A

27791810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125480610-T-G

27792081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125480907-C-T

27792106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125480929-C-T

27792468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125481183-C-T

27792544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125481261-T-C

27792993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125481464-T-C

27793030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125481479-C-T

27793091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125481535-A-G

27793091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125481535-A-T

27793641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125482066-G-A

27793778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125482196-C-T

27793960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125482376-G-T

27795752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125483922-T-C

27795762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125483940-G-A

27795762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125483940-G-T

27798466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125485367-G-A

27798532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125485430-G-A

http://identifiers.org/hco/16/GRCh38#27798918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125485798-A-C

27800069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125486464-T-C

27800835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125487199-A-G

27801216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125487457-A-G

27801268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125487510-G-A

27801337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125487562-A-G

http://identifiers.org/hco/16/GRCh38#27801485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125487703-C-A

27801485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125487703-C-T

27802455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125488843-G-A

27806713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125490317-G-A

27806793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125490360-C-G

http://identifiers.org/hco/16/GRCh38#27806797-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125490364-A-C

27806917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125490468-G-A

27807475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125490820-C-G

27807503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: synonymous variant
orthologous variants: 125490848-G-A

27807503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: missense variant
orthologous variants: 125490848-G-C

27807593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125490935-G-T

http://identifiers.org/hco/16/GRCh38#27807594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125490936-A-C

27807594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125490936-A-G

27807608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125490950-G-C

27807608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125490950-G-T

http://identifiers.org/hco/16/GRCh38#27807638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125490982-C-A

27807638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125490982-C-T

27807639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125490983-A-G

27807640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125490984-A-G

27817359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125493290-C-T

27817433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125493347-C-T

27817434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125493348-A-G

27818083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125494126-C-G

27818310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125494307-C-T

27818358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125494353-T-C

http://identifiers.org/hco/16/GRCh38#27818394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125494397-C-A

27818394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125494397-C-T

27818409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125494416-C-T

27818527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125494531-C-T

http://identifiers.org/hco/16/GRCh38#27818730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125494712-C-A

27818880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125494850-C-T

http://identifiers.org/hco/16/GRCh38#27820436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125496387-A-C

27820615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125496554-T-C

27820678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125496612-G-A

27820678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125496612-G-C

27822237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125497703-G-A

27822418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125497850-G-A

27822639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125498119-G-A

27822697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125498198-C-T

27822871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125498377-T-C

http://identifiers.org/hco/16/GRCh38#27823070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125498582-C-A

27823339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125498868-A-G

27823473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: intron variant
orthologous variants: 125498994-G-A

http://identifiers.org/hco/16/GRCh38#27824011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125499481-A-C

27824011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125499481-A-G

27824567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125499962-A-G

27824707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125500105-T-C

27824731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125500129-T-C

http://identifiers.org/hco/16/GRCh38#27826141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125500635-A-C

27826261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125500742-G-A

http://identifiers.org/hco/16/GRCh38#27826318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125500783-A-C

27826318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125500783-A-G

27826391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125500825-C-T

27826443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125500874-C-T

27826533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125500951-G-A

27826864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125501241-T-G

27826892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125501256-A-T

27827363-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125508258-T-G

27827885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125508479-T-A

27827885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125508479-T-C

http://identifiers.org/hco/16/GRCh38#27827907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125508498-C-A

http://identifiers.org/hco/16/GRCh38#27827916-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125508507-A-C

27827916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125508507-A-G

27827994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125508586-T-A

27827994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125508586-T-C

27827994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125508586-T-G

27828240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125508835-T-A

27828240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125508835-T-G

27828401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125508995-C-T

27828976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125509569-G-A

27828976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125509569-G-C

27828993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125509586-G-A

27828993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125509586-G-T

http://identifiers.org/hco/16/GRCh38#27829042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125509629-C-A

27829042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125509629-C-T

27829403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125509917-G-A

27829856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125510148-T-C

27830470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125510667-C-T

27830829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125511049-G-T

27830854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125511076-A-G

27831090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125511273-G-A

27831163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125511336-A-G

27831187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125511356-G-A

27831285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125511439-A-G

27831342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125511484-G-A

http://identifiers.org/hco/16/GRCh38#27831359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125511501-A-C

27831391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125511533-A-G

27831400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125511542-T-A

http://identifiers.org/hco/16/GRCh38#27831437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125511577-C-A

27831523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125511666-T-C

http://identifiers.org/hco/16/GRCh38#27831728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125512845-A-C

http://identifiers.org/hco/16/GRCh38#27831901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125512987-C-A

27832154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125513163-T-A

27832372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125513385-C-T

27832457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125513474-A-G

27832487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125513504-G-A

27832708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125513693-A-G

27833099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125514385-A-T

27833312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125514552-G-A

27833421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125514720-G-C

27833744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125515118-C-T

27833822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125515189-G-T

27833846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125515211-T-C

27833846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125515211-T-G

27833919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125515281-A-G

27834015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125515335-C-T

27834037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125515353-T-C

27834405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125515738-C-T

27834947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125516286-G-C

27834947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125516286-G-T

27837982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125518105-C-T

27838090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125518224-G-A

27838585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125518653-G-A

27838605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125518673-C-T

27839120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125519074-A-G

http://identifiers.org/hco/16/GRCh38#27839343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125519355-C-A

27839343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125519355-C-T

27839472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125519494-A-G

27839518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125519522-A-T

27839703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125519640-T-C

27839857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125519783-G-A

27840834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125520425-C-G

27840834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125520425-C-T

27840838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125520429-C-T

27841113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125520638-A-G

27841179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125520700-G-A

http://identifiers.org/hco/16/GRCh38#27841249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125520767-A-C

27841385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125520854-G-A

27841388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125520857-T-C

27841448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125520900-G-A

27841448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125520900-G-T

27841463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125520913-G-T

27841542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125520979-G-A

27841616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125521050-G-A

27841749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125521172-T-C

27841985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125521396-G-A

http://identifiers.org/hco/16/GRCh38#27843350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125521816-A-C

27843350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125521816-A-T

http://identifiers.org/hco/16/GRCh38#27843376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125521843-C-A

27843376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125521843-C-G

27843381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125521848-G-A

http://identifiers.org/hco/16/GRCh38#27843426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125521885-C-A

27843426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125521885-C-G

27843426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125521885-C-T

27843613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522015-G-C

27843613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522015-G-T

27843640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522041-C-T

27843890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522283-A-G

27843908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522301-A-T

http://identifiers.org/hco/16/GRCh38#27844892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125522548-C-A

27844892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522548-C-G

27844892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522548-C-T

http://identifiers.org/hco/16/GRCh38#27844897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125522553-C-A

27844897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522553-C-T

http://identifiers.org/hco/16/GRCh38#27844902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125522558-C-A

27844902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522558-C-T

27844936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522581-G-A

27844936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522581-G-T

27845009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 125522654-G-A

27845009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 125522654-G-C

27845009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 125522654-G-T

27845065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 125522710-T-C

27845066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 125522711-G-T

27845101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522738-G-A

27845101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522738-G-T

http://identifiers.org/hco/16/GRCh38#27845121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125522770-A-C

http://identifiers.org/hco/16/GRCh38#27845122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125522771-C-A

27845122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125522771-C-T

27846551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125527985-C-T

27846682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125528109-C-T

27846683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125528110-G-A

27851777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125530169-T-C

http://identifiers.org/hco/16/GRCh38#27851846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125530211-A-C

27851846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125530211-A-G

27851886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125530255-C-T

27851892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125530261-G-A

27852412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125531927-C-T

http://identifiers.org/hco/16/GRCh38#27852782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125532272-C-A

http://identifiers.org/hco/16/GRCh38#27852807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125532317-A-C

27852832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125532387-G-A

27853496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125532910-G-A

27854354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125533718-G-A

27854412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125533798-C-T

27854413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125533799-A-G

27856822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125535181-A-G

http://identifiers.org/hco/16/GRCh38#27856825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125535184-C-A

27856829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125535188-T-A

27856829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125535188-T-C

27856835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125535194-A-T

27857448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125535621-A-G

27857565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125535641-A-G

http://identifiers.org/hco/16/GRCh38#27857612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125535676-A-C

27857713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125535754-T-C

27858033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125536023-C-T

27858249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125536158-A-G

27858315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125536210-T-C

27860623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125536650-T-C

27861411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125536844-A-G

27861628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125537059-C-T

http://identifiers.org/hco/16/GRCh38#27861696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125537117-C-A

27862483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125538139-A-G

27862809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125538604-G-A

27862809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125538604-G-T

27862910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125538698-T-C

27862952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125538744-G-A

http://identifiers.org/hco/16/GRCh38#27863066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125538803-C-A

27863162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125538965-A-T

27863397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125539064-C-G

27863397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125539064-C-T

http://identifiers.org/hco/16/GRCh38#27863398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125539065-C-A

27863412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125539079-T-C

http://identifiers.org/hco/16/GRCh38#27863432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125539099-C-A

27863557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125539202-A-G

27863734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125539354-C-T

27863745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125539365-C-T

27863797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125539415-T-A

27863834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125539451-T-C

27863899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125539516-C-G

27863943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125539555-A-G

27864091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125539673-C-T

27864325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125539842-G-T

27864607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125540098-C-T

27864639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125540130-T-A

27864665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125540152-G-T

27864841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125540299-C-G

27864841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125540299-C-T

27865137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125540525-C-T

27865219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125540595-G-A

27865266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125540626-C-T

http://identifiers.org/hco/16/GRCh38#27865419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#125540793-C-A

27867154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125541261-C-T

27867591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125541564-G-A

27867607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125541580-C-T

27867716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125541679-A-T

27867959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125541766-T-C

27867984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125541790-T-G

27868370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125542142-A-G

27868535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125542288-A-G

27872004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125544985-G-C

27872191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125545215-T-G

27872274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125545294-T-C

27872318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125545332-C-G

27872318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125545332-C-T

27874973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125546924-A-G

27875071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125547013-T-C

27875084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125547026-G-A

27875095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125547037-G-C

27875208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125547126-G-T

http://identifiers.org/hco/16/GRCh38#27875359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125547259-C-A

27875531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125549608-C-T

27875588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125549666-G-A

27875775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125549728-T-C

27875822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125549757-T-C

27875847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125549772-T-C

27875955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125549859-T-C

27875967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125549871-T-G

http://identifiers.org/hco/16/GRCh38#27876119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125550482-C-A

27876123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125550486-T-C

http://identifiers.org/hco/16/GRCh38#27876398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125550754-C-A

27876398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125550754-C-T

27876463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125550815-G-A

27876635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125550977-C-T

27876651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125550993-T-C

27876670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125551012-G-A

27876703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125551031-C-T

27876722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125551047-C-T

27876737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125551062-T-C

27876766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125551093-G-C

27876786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125551106-T-C

27876882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125551183-G-C

27877867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125553068-C-T

27877876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125553077-A-T

27880215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125554023-A-G

27880674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125554465-C-T

27880691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125554481-G-T

27883261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125556592-G-T

27883295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125556618-G-A

27883426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125556672-T-C

27883760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125556962-G-A

27884574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 125557695-G-A

27884627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 125557748-G-A

27884627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 125557748-G-C

27884627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 125557748-G-T

27884633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 125557754-G-A

27884754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125557854-G-A

27884754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125557854-G-T

27884960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125557898-G-A

27885763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125558340-A-T

27893029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125563622-C-T

27893377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125563951-G-C

27894316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125565393-A-T

27894553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125565623-G-A

27894747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125565812-C-T

27894768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125565830-A-G

27895003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125566024-C-T

27895271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125566289-A-G

27895365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125566385-G-A

27895371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125566391-C-T

27895462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125566459-T-G

http://identifiers.org/hco/16/GRCh38#27895681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125567097-C-A

http://identifiers.org/hco/16/GRCh38#27895854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125567258-A-C

27895856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125567260-C-G

27895856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125567260-C-T

http://identifiers.org/hco/16/GRCh38#27896087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125567475-A-C

27897959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125568238-G-A

27898246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125568515-G-A

27898285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125568550-T-C

27898366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125568624-A-G

27898390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125568645-A-T

27898398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125568653-A-T

27898562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125568775-C-T

27898882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125568957-A-T

27898993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125569035-T-C

27899065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125569121-T-C

27899076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125569133-C-T

27906607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125572151-C-T

27906722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125572241-C-T

http://identifiers.org/hco/16/GRCh38#27906796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125572292-A-C

27906796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125572292-A-G

http://identifiers.org/hco/16/GRCh38#27906921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125572392-C-A

27906921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125572392-C-T

27907002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125572472-T-G

27907535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125572900-T-G

27907563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125572935-C-T

27907588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125572962-G-T

27907939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125573251-T-C

27908363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125573607-G-A

27908552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125573793-A-G

27912117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125575390-C-T

27913179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125575894-A-G

27913200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125575909-A-G

27913252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125575961-T-C

27913281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125575979-A-T

27913348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125576028-G-A

27913390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125576066-A-G

27913539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125576228-G-T

27913544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125576232-T-C

27913890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125577098-G-A

27913890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125577098-G-C

27913981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125577193-C-T

27914024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125577226-G-A

http://identifiers.org/hco/16/GRCh38#27914161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125577361-C-A

27914279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125577478-A-T

http://identifiers.org/hco/16/GRCh38#27914489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125577654-A-C

27914642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125577713-A-G

http://identifiers.org/hco/16/GRCh38#27914661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125577728-C-A

27914661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125577728-C-T

27914935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125577976-A-G

27915131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125578141-G-A

27915132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125578142-C-T

27915136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125578148-T-C

27915140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125578151-T-C

27915147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125578158-A-G

27915169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125578181-C-T

27915195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125578213-G-T

27915198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125578216-C-T

27915266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125578244-A-G

27915285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125578263-A-T

27915289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125578267-T-C

27915289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125578267-T-G

27915308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125578288-G-T

27916840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125579084-G-C

27916996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125579212-G-A

27917327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125579555-G-A

27917422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125579625-G-A

27917439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125579642-G-C

27917610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125579823-C-T

27917964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125580173-G-T

27918946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125581062-C-T

27919006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125581129-G-A

27919006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125581129-G-C

27919329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125581445-T-C

27919356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125581471-C-G

27919700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125581760-C-T

http://identifiers.org/hco/16/GRCh38#27919749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125581807-C-A

27920256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125582922-C-G

27920256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125582922-C-T

http://identifiers.org/hco/16/GRCh38#27920304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125582969-C-A

27921176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125583800-G-T

27921664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125584271-T-C

27921777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125584396-T-C

27921834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125584432-C-T

27922017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125584530-G-C

27922017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125584530-G-T

http://identifiers.org/hco/16/GRCh38#27922021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125584534-C-A

27922021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125584534-C-T

27922024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125584537-G-T

27925720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125587058-C-G

27926278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125587659-G-A

27931168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125591711-G-C

27931477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125592007-C-G

27932703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125594699-C-T

27932732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125594722-T-G

27932767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125594756-T-C

27932812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125594799-C-T

27932924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125594906-C-T

27933020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125595019-G-A

27933294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125595300-G-T

27935377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125600295-G-A

27935517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125600403-C-T

27935994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125601064-C-T

27938689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125601427-G-A

27938736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125601473-G-C

27938850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125601561-G-A

27938864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125601575-G-A

27938957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125601653-T-C

27939694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125602293-A-G

27945993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125608215-A-G

27950547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125612110-G-A

27950740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125612305-A-G

27950750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125612315-A-G

27951727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125613124-G-A

27951727-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125613124-G-C

27951820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125613218-C-T

27951955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125613304-T-C

27955839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125614993-T-C

27955908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125615107-G-A

27955978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125615177-G-A

27955978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125615177-G-C

http://identifiers.org/hco/16/GRCh38#27956385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125615759-C-A

27956452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125615829-C-T

27956742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125616082-T-A

27956742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125616082-T-C

27956743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125616083-C-G

27956975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125616273-G-A

27957020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125616320-G-T

27960595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125618548-T-C

27960634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125618585-G-A

27960698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125618653-G-T

http://identifiers.org/hco/16/GRCh38#27960790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125618736-C-A

27960790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125618736-C-T

http://identifiers.org/hco/16/GRCh38#27960803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125618749-A-C

27960819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125618764-G-C

27961063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125618994-G-A

27961151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125619058-G-T

27961212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125619109-G-A

27961228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125619126-A-G

27962959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125619643-C-T

27963006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125619692-G-A

27963006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125619692-G-T

27963097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125619757-T-A

27963097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125619757-T-C

27963166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 125619806-T-A

27963166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 125619806-T-C

27963172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 125619812-G-A

27963172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 125619812-G-C

27963172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 125619812-G-T

27963241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125619879-G-T

http://identifiers.org/hco/16/GRCh38#27963295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125619927-C-A

27963295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125619927-C-T

27963498-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125620102-C-G

27963543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125620137-G-A

27963776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125620346-G-C

27967256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125620392-T-A

27967256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125620392-T-C

27967468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125620593-G-A

27967512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125620637-A-G

27967513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125620638-T-C

http://identifiers.org/hco/16/GRCh38#27967540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125620665-C-A

27971852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125625236-T-C

27971938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125625314-C-T

27972076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125625445-C-T

27972374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125625719-G-A

27972721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125626053-C-G

27972721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125626053-C-T

27972766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125626084-T-C

27972769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125626087-G-A

27972769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125626087-G-T

27972807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125626096-T-G

27972842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125626132-T-A

27974154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125626251-G-C

27974358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125626387-G-A

27974358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125626387-G-C

27974433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125626442-T-G

27974434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125626443-T-G

27974630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125626602-C-T

http://identifiers.org/hco/16/GRCh38#27974741-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125626695-A-C

27974769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125626722-G-A

27976778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -G-A

http://identifiers.org/hco/16/GRCh38#27976810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -A-C

27976810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -A-T

27976832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-T

27976834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-T

27976848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -G-A

27980015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125630802-T-C

27980015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125630802-T-G

27980114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125630898-G-A

27980114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125630898-G-T

27981409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125632020-A-T

27981777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125632391-A-G

27994372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125634612-T-C

27994571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125634832-C-G

27994573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125634834-C-T

27994861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125635327-T-C

27994861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125635327-T-G

27994872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125635338-G-C

27994920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125635381-A-G

27995105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125635561-A-T

27995377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125635817-C-G

27995431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 125635856-T-C

27995487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125635908-G-T

27995918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125636024-A-G

27995932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125636039-G-C

http://identifiers.org/hco/16/GRCh38#27995939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125636046-C-A

http://identifiers.org/hco/16/GRCh38#27996065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125636201-C-A

27996262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125636302-A-G

28000168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125637588-G-A

28000437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125637675-C-T

28000583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125637816-T-G

28000711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125637952-T-C

28000937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125638247-C-T

http://identifiers.org/hco/16/GRCh38#28001011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125638314-A-C

28001077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125638364-A-T

28001399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125638672-C-T

28002176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125639341-G-A

28002184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125639349-T-C

http://identifiers.org/hco/16/GRCh38#28002318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125639484-C-A

28003308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125639820-G-A

28003308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125639820-G-C

28003317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125639829-G-A

28003333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125639844-G-A

28003399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125639923-G-T

http://identifiers.org/hco/16/GRCh38#28003602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125640072-C-A

28003606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125640076-C-T

28003612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125640082-C-T

28003793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125640240-A-G

28003915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125640333-G-T

http://identifiers.org/hco/16/GRCh38#28004332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125640650-A-C

28004422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125640736-G-A

28004422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125640736-G-C

28006736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125641659-A-G

28006791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125641709-G-T

28007145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125642060-A-G

28007162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125642076-G-T

http://identifiers.org/hco/16/GRCh38#28009371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125644467-C-A

http://identifiers.org/hco/16/GRCh38#28009383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125644479-C-A

http://identifiers.org/hco/16/GRCh38#28009428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125644512-C-A

28009621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125644704-A-G

http://identifiers.org/hco/16/GRCh38#28009643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125644726-A-C

28009898-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125644869-A-T

http://identifiers.org/hco/16/GRCh38#28009975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125644927-C-A

28009975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125644927-C-T

28009985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125644932-A-T

http://identifiers.org/hco/16/GRCh38#28009999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125644941-A-C

28010182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645094-T-C

28010184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645096-G-A

28010228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645139-G-A

28010228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645139-G-C

28010228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645139-G-T

28010293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645204-C-T

28010337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645242-G-C

28010511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645396-C-G

28010750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645628-A-G

28010817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645671-A-G

28010836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645689-T-G

http://identifiers.org/hco/16/GRCh38#28010924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125645769-C-A

28011043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645911-A-G

28011086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645951-T-C

28011086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125645951-T-G

28011293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125646079-C-T

28011449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125646192-G-A

28011480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125646222-C-T

28011518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125646257-G-T

28011521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125646260-G-A

28011534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125646272-G-A

28011907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125646608-C-T

28012232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125646877-C-T

28012261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125646906-G-C

28012407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125647055-G-A

28012421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125647069-A-G

http://identifiers.org/hco/16/GRCh38#28016859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125648705-A-C

28016940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125648785-G-A

28016988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125648833-C-T

28017009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125648850-G-A

28017013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125648854-G-A

28017013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125648854-G-C

28017100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125648943-G-T

28017191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125649033-A-G

http://identifiers.org/hco/16/GRCh38#28017217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125649059-A-C

28017302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125649143-G-C

28017473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125649267-C-T

28017482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125649276-G-A

28017711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125649500-A-G

28020152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125649551-A-G

28020260-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125649655-C-G

28024338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125650165-G-A

http://identifiers.org/hco/16/GRCh38#28024380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125650187-C-A

28024380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125650187-C-T

28024467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125650287-C-T

28024516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125650341-C-T

28024517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125650342-G-A

28024517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125650342-G-T

28024563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125650377-C-T

28024843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125650616-G-A

28024951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125650720-A-G

28025128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125650855-G-A

28025280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125650988-G-T

28025697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125651389-G-A

28025714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125651406-G-A

28026090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125651772-G-A

28026111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125651786-G-T

28026182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125651857-G-A

28027412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125652918-G-T

28027420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125652926-G-T

28027425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125652931-G-A

28027442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125652948-C-T

http://identifiers.org/hco/16/GRCh38#28028036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125653317-A-C

http://identifiers.org/hco/16/GRCh38#28028422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125653633-C-A

28028422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125653633-C-T

28028889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125654090-G-A

28031606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125655517-C-T

28032121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125656619-G-A

http://identifiers.org/hco/16/GRCh38#28032176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125656689-C-A

28032176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125656689-C-G

28032176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125656689-C-T

28032384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125656872-G-A

28032384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125656872-G-T

28032456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125656926-G-A

28032456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125656926-G-T

28032545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125656985-T-G

28032908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125657238-G-A

28032969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125657295-T-C

http://identifiers.org/hco/16/GRCh38#28033214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125657503-C-A

28033214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125657503-C-T

28033539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125657905-G-A

28033791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125658131-A-G

28033912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125658254-A-G

28034032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125658361-G-A

28037451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125660407-T-G

28037555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125660505-A-G

28037649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125660603-A-G

28037806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125660743-G-A

28037853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125660784-T-C

28038291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125661315-C-T

28038521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125661523-G-A

28038641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125661633-G-A

28038718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125661702-C-T

28038745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125661728-T-C

28038764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125661748-G-C

28038838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125661813-C-T

28038932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125661909-G-C

28038932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125661909-G-T

28039094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125662114-T-C

http://identifiers.org/hco/16/GRCh38#28039243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125662235-A-C

28039586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125662548-T-A

28039586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125662548-T-C

28039658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125662612-C-T

28039738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125662687-A-G

28039957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125662901-C-T

28040099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125663034-G-A

28040128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125663062-C-T

28040213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125663124-G-A

28040213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125663124-G-T

28040246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125663157-G-A

28042749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125666004-G-A

28042806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125666046-A-G

28042810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125666050-T-C

28043015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125666255-A-G

28043045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125666284-C-G

28047198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125669428-C-T

28047794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125670735-G-A

28047912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125670845-A-G

28048888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125671756-A-G

28054057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125673510-G-A

28054057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125673510-G-C

28054189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125673604-G-A

http://identifiers.org/hco/16/GRCh38#28054220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125673643-C-A

http://identifiers.org/hco/16/GRCh38#28054265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125673703-C-A

28059066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125678199-G-T

28059120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125678240-C-T

28059130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125678250-C-T

http://identifiers.org/hco/16/GRCh38#28059566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125678614-C-A

http://identifiers.org/hco/16/GRCh38#28059640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125678670-C-A

28059861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125678856-G-A

28059960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125678934-G-A

28059960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125678934-G-C

28059960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125678934-G-T

28060443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125679366-G-A

28060548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125679472-T-C

28060625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125679546-C-T

28060940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125679881-A-G

28060998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125679953-G-T

28061042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125679989-A-G

28062398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125680587-A-G

28062486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125680693-G-A

http://identifiers.org/hco/16/GRCh38#28062543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125680731-C-A

28062543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125680731-C-T

28062714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125680880-G-C

28062765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125680930-G-T

http://identifiers.org/hco/16/GRCh38#28063062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#125681018-C-A

28063062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125681018-C-G

28063062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125681018-C-T

28063149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 125681105-G-A

28063149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 125681105-G-C

28063149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28283
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 125681105-G-T