27325357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34949227-T-C

27325435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34949300-T-C

http://identifiers.org/hco/9/GRCh38#27325627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34949488-C-A

http://identifiers.org/hco/9/GRCh38#27325779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34949590-C-A

27325779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34949590-C-G

27325824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34949612-T-C

27326259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34949937-G-T

27326277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34949955-A-G

27326336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34950011-A-G

27326530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34950199-A-T

27326654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34950317-G-T

27326726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34950368-G-A

http://identifiers.org/hco/9/GRCh38#27327367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34950839-C-A

27327367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34950839-C-T

27327508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34950983-T-C

27327540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951013-G-A

27327540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951013-G-T

http://identifiers.org/hco/9/GRCh38#27327546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34951019-C-A

http://identifiers.org/hco/9/GRCh38#27327555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34951028-C-A

27327555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951028-C-T

27327556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951029-A-G

http://identifiers.org/hco/9/GRCh38#27327615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34951064-C-A

27327615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951064-C-T

27327684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951127-G-T

27327763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951213-T-G

27327802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951257-G-A

http://identifiers.org/hco/9/GRCh38#27328006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34951383-A-C

http://identifiers.org/hco/9/GRCh38#27328090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34951403-C-A

27328115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951428-C-T

27328121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951434-A-G

27328178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951473-C-T

27328192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951487-G-A

27328245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951532-T-C

27328248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951535-G-A

27328249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951536-T-C

27328289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951580-T-C

27328335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951624-G-T

27328401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951682-A-G

27328485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951760-T-G

27328562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951844-T-A

27328567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951849-A-G

27328570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951852-G-C

27328583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951865-A-G

27328585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951867-C-G

27328613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951895-T-C

27328621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951903-C-T

27328622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951904-A-G

27328660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951942-A-G

27328665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951947-G-C

27328665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951947-G-T

27328674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951956-C-T

27328683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951965-T-A

27328683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34951965-T-C

27328759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952049-G-T

27328762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952052-G-T

http://identifiers.org/hco/9/GRCh38#27328816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34952102-C-A

27328836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952161-A-G

27328951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952414-G-A

27328951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952414-G-T

27329014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952502-G-A

27329014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952502-G-T

27329023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952511-C-T

http://identifiers.org/hco/9/GRCh38#27329025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34952513-C-A

27329039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952562-T-C

27329382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952876-T-C

27329407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952901-A-G

http://identifiers.org/hco/9/GRCh38#27329456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34952930-C-A

27329487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952960-G-A

27329487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952960-G-T

27329512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34952997-G-A

27329524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953009-G-A

27329524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953009-G-T

http://identifiers.org/hco/9/GRCh38#27329559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953047-A-C

27329559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953047-A-T

27329574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953062-G-A

27329574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953062-G-T

27329581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953069-G-C

27329637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953108-A-T

27329666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953142-C-T

http://identifiers.org/hco/9/GRCh38#27329731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953208-C-A

27329757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953225-T-A

27329782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953250-A-G

27329800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953268-G-C

27329800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953268-G-T

27329815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953283-T-C

27329815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953283-T-G

http://identifiers.org/hco/9/GRCh38#27329887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953364-C-A

27329925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953402-A-G

27329925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953402-A-T

27329938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953415-T-C

27329938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953415-T-G

27329949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953431-T-A

27329949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953431-T-C

27329974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953456-G-A

27329974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953456-G-T

27329977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953459-A-G

27329995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953475-A-G

http://identifiers.org/hco/9/GRCh38#27330055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953507-C-A

http://identifiers.org/hco/9/GRCh38#27330070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953522-C-A

27330164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953611-A-G

27330164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953611-A-T

http://identifiers.org/hco/9/GRCh38#27330171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953618-C-A

27330171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953618-C-G

27330194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953637-T-C

http://identifiers.org/hco/9/GRCh38#27330205-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953648-A-C

27330205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953648-A-G

http://identifiers.org/hco/9/GRCh38#27330231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953677-C-A

27330250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953696-T-C

27330250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953696-T-G

http://identifiers.org/hco/9/GRCh38#27330252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953698-C-A

27330299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953745-G-A

27330299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953745-G-T

27330304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953750-T-A

27330304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953750-T-C

http://identifiers.org/hco/9/GRCh38#27330306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953752-C-A

27330306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953752-C-T

http://identifiers.org/hco/9/GRCh38#27330336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953780-C-A

27330368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953806-G-A

27330368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953806-G-C

27330368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953806-G-T

http://identifiers.org/hco/9/GRCh38#27330405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953843-C-A

27330405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953843-C-T

http://identifiers.org/hco/9/GRCh38#27330425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953863-C-A

27330439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953877-G-A

27330439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953877-G-C

27330439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953877-G-T

27330444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953882-G-A

27330444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953882-G-T

27330493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953925-G-A

27330493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953925-G-C

27330493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953925-G-T

27330512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953943-G-A

27330512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953943-G-C

27330527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953958-G-T

http://identifiers.org/hco/9/GRCh38#27330549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34953980-A-C

27330549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953980-A-G

27330549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3 prime UTR variant
orthologous variants: 34953980-A-T

http://identifiers.org/hco/9/GRCh38#27330684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34954109-C-A

http://identifiers.org/hco/9/GRCh38#27330733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34954125-C-A

27330733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34954125-C-T

27330764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34954136-T-C

http://identifiers.org/hco/9/GRCh38#27330828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34954336-C-A

27330930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34954448-A-G

27330934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34954452-G-T

http://identifiers.org/hco/9/GRCh38#27331162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34954682-C-A

27331211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34954729-A-G

27331257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34954776-T-C

27331264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34954785-C-T

27331282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34954801-C-T

27331367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34954866-G-A

http://identifiers.org/hco/9/GRCh38#27331372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34954871-C-A

27331418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34954906-C-T

27331480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34954956-G-A

27331480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34954956-G-T

27333782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34959612-G-C

27334040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34959877-C-T

27334108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34959934-G-A

27334183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34960013-T-C

http://identifiers.org/hco/9/GRCh38#27334347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34960174-A-C

27334520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34960346-G-T

27334596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34960416-A-G

27336495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34961215-C-T

27336507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34961225-G-A

27336509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34961231-G-A

27336513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34961235-G-A

27336520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34961242-C-T

27336576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34961294-G-A

27336591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34961307-C-T

27337177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34961850-C-T

27337555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34962184-C-T

27337831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34962410-T-C

27339205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34963902-C-G

27339278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34963951-T-C

27339396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34964078-G-A

27339420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34964105-G-A

27339499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34964157-C-T

27339557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34964203-A-G

27339647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34964267-G-C

27339719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34964342-C-T

27339741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34964364-A-G

27339741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34964364-A-T

27339804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34964418-C-T

27340015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34964639-T-C

27340155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34964775-G-A

27340283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34964900-A-G

27340383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34965002-T-C

27340445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34965064-C-G

27340461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34965075-A-G

27340483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34965097-G-A

27340484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34965098-T-G

27340606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34965618-T-A

27340671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34965683-G-A

27340714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34965741-C-T

27340860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34966611-G-T

http://identifiers.org/hco/9/GRCh38#27340871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34966622-C-A

27340921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34966681-T-C

27341063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34966814-G-A

27341306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34967017-C-T

27341357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34967088-C-T

http://identifiers.org/hco/9/GRCh38#27341463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34967190-C-A

27341881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34968193-C-T

27342084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34968857-A-G

27342091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34968864-T-C

27342140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34968910-C-T

27342154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34968943-G-A

27342158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34968947-T-C

27342192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34968982-C-T

27342249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34969037-G-A

27342358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34969123-A-T

27343746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34969385-G-T

27343754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34969393-A-T

27343813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34969432-G-A

27343912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34970203-T-C

27343918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34970209-T-C

27344006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34970302-A-G

27344037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34970344-C-G

27344185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34970469-T-C

27344333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34970647-C-T

27344363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34970681-G-T

27344456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34970964-T-G

27344475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34970983-C-T

27344496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34971004-C-T

27344528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34971036-A-G

27344609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34971122-C-T

27344611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34971124-A-G

27344617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34971130-A-T

27344654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34971158-G-A

27344715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34971215-G-A

27344963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34971449-G-A

27344989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34971475-C-T

http://identifiers.org/hco/9/GRCh38#27345066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34971553-C-A

27345114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34971602-C-G

27347124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34972082-G-A

http://identifiers.org/hco/9/GRCh38#27348019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34975223-C-A

27349075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34976011-A-G

27349183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34976114-C-T

27349292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34976204-C-T

27349629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34976535-T-G

27349757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34976662-G-A

27350053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34976909-G-A

http://identifiers.org/hco/9/GRCh38#27350284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34979674-C-A

27350304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34979694-C-T

http://identifiers.org/hco/9/GRCh38#27350401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34979794-C-A

27350597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34979992-T-C

27350597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34979992-T-G

27350634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34980009-G-T

27350644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34980019-T-C

27350729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34980096-C-T

27351110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34980278-C-G

27351205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34980301-C-T

27351209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34980305-G-C

27351243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34980339-A-G

27351292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34980388-T-C

27351340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34980416-A-T

http://identifiers.org/hco/9/GRCh38#27351541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34980591-C-A

27351548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34980598-G-A

27351624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34980674-C-T

27351791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34980839-G-A

27353228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34981195-C-T

27353274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34981241-C-T

27353399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34981361-T-C

27353399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34981361-T-G

27353404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34981366-T-C

27353661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34981578-C-T

http://identifiers.org/hco/9/GRCh38#27353739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34981640-A-C

27353741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34981642-T-A

27353819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 34981722-A-G

27353874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34981776-A-T

27354011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34981915-C-G

27354011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34981915-C-T

http://identifiers.org/hco/9/GRCh38#27354095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#34981981-C-A

27354240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34982060-T-G

http://identifiers.org/hco/9/GRCh38#27354261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34982081-C-A

27354413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34982226-T-C

27354421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34982234-A-G

27354785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34982570-C-T

27355069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34982836-C-T

27356084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34983109-A-T

27356090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34983115-C-T

27356152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34983179-T-C

27356191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34983204-T-A

27356310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34983315-C-G

27356310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34983315-C-T

27356329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34983330-T-C

27356704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34983722-G-A

http://identifiers.org/hco/9/GRCh38#27356711-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34983729-A-C

27356711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34983729-A-T

http://identifiers.org/hco/9/GRCh38#27356873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34983862-C-A

27356873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34983862-C-G

27356877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34983866-C-T

http://identifiers.org/hco/9/GRCh38#27356882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34983871-C-A

27356948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34983961-T-A

27357169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34984319-T-A

http://identifiers.org/hco/9/GRCh38#27357174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34984323-C-A

27357182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34984331-T-C

27357214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34984361-G-A

http://identifiers.org/hco/9/GRCh38#27357315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34984462-C-A

27357332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34984479-G-T

27357502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34984649-T-C

27357649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34984749-C-T

27357690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34984770-G-A

27358616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34985581-C-G

27358774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34985716-C-G

27358774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34985716-C-T

27358830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34985780-G-C

27358830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 34985780-G-T

http://identifiers.org/hco/9/GRCh38#27358893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34985824-C-A

27359043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34985925-T-C

27359169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34986051-A-G

27359250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986132-A-G

27359300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986179-C-T

27359306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986187-T-C

27359313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986195-T-C

http://identifiers.org/hco/9/GRCh38#27359336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34986218-A-C

27359336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986218-A-T

27359477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986303-G-A

27359731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986552-C-G

27360014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34986815-A-G

27360480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34987015-T-C

27360480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34987015-T-G

27360592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34987075-T-C

27360613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34987096-A-G

27360759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34987258-C-T

27360985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34987470-C-T

27361162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34987594-G-C

27361228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34987653-T-G

27361270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34987693-G-A

http://identifiers.org/hco/9/GRCh38#27361308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34987733-C-A

27361308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34987733-C-T

27361628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34988067-A-G

27361714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34988142-G-A

http://identifiers.org/hco/9/GRCh38#27361721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34988149-C-A

27361769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34988196-A-G

27361800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34988230-A-T

27361983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34988422-A-G

27362021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34988462-C-T

27362780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34988644-T-C

27363202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34988924-T-A

27363230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34988952-C-T

27364267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34989489-A-G

27364267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34989489-A-T

27364677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34989803-A-G

http://identifiers.org/hco/9/GRCh38#27364808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34989941-C-A

http://identifiers.org/hco/9/GRCh38#27364826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34989955-A-C

27364998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34990330-G-A

27364998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34990330-G-C

27365020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34990352-C-T

27365116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34990449-C-T

27365236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34990550-T-C

27365275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34990591-T-G

27365394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34990694-G-T

27365440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34990743-A-T

http://identifiers.org/hco/9/GRCh38#27365447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34990750-A-C

27365458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34990761-C-T

27365459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34990762-T-C

27365459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34990762-T-G

27365482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34990835-G-T

27365674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34991012-C-T

http://identifiers.org/hco/9/GRCh38#27365890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34991207-C-A

27365973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34991287-G-C

27366454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34991718-A-G

27366455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34991719-T-C

27366533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34991853-G-A

27366651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34991938-C-T

http://identifiers.org/hco/9/GRCh38#27366680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34991959-C-A

27366680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34991959-C-T

27367041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34992069-C-T

27367094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34992111-T-C

27367261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34992287-C-G

27367520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34992546-C-T

27367588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34992625-T-C

27367692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34992705-G-A

27367862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34992861-G-A

27367862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34992861-G-C

27367875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34992871-T-C

27367960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34992959-T-C

27367967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34992966-G-A

27368060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34993062-T-C

27368849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34993771-G-A

27368948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34993871-T-C

27369050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34993961-G-A

27369239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34994099-G-T

27369291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34994150-C-G

27369409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34994297-A-G

27369442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34994337-C-T

27369682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34994562-G-A

27369699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34994579-T-C

27370792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34996073-G-C

27370852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34996112-C-T

27370949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34996237-C-T

27370997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34996274-C-T

27371043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34996313-G-T

http://identifiers.org/hco/9/GRCh38#27371100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34996370-A-C

27371265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34996625-T-C

http://identifiers.org/hco/9/GRCh38#27371368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34996755-C-A

27371379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34996766-T-C

27371523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34996882-G-T

http://identifiers.org/hco/9/GRCh38#27371546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34996904-C-A

27371546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34996904-C-T

27371689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34997061-T-C

27371702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34997074-C-T

27372000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34997473-A-G

27372031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34997562-C-T

27372046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34997589-G-A

http://identifiers.org/hco/9/GRCh38#27372094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34997653-A-C

27372111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34997670-T-A

27372200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34997748-T-C

http://identifiers.org/hco/9/GRCh38#27372353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#34998090-A-C

27372422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34998164-C-T

27372573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34998307-G-A

27372626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34998367-C-T

27372651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34998390-C-T

27372839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34998677-A-G

27374284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34999350-G-A

27374422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34999482-T-C

27374702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34999738-C-T

27374709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34999746-T-A

27374808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34999831-G-A

27374865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34999894-A-G

27374888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34999917-C-T

http://identifiers.org/hco/9/GRCh38#27375188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35000807-C-A

27375188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35000807-C-T

27375210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35000828-T-C

27375296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35000905-T-C

27375375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35000979-T-C

27375376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35000980-G-A

27375394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35000998-T-C

27375420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35001008-A-G

http://identifiers.org/hco/9/GRCh38#27375506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35001085-A-C

27375652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35001221-T-C

27375849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35001400-A-G

27375921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35001474-T-G

27376100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35001801-G-T

27376285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35002139-A-G

27376355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35002201-T-A

27376355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35002201-T-G

27376448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35002271-G-A

27376554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35002369-G-A

27376749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35002516-G-A

27377085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35002790-G-T

27377155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35002876-T-C

27377166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35002887-A-G

27379326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35003444-C-T

27379500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35003574-C-T

27379898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35003953-T-C

27380107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35004157-T-C

27380145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35004195-C-G

27380145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35004195-C-T

27380172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35004217-T-G

27380248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35004291-G-A

27380261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35004304-G-A

27380261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35004304-G-C

27381086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35004737-T-C

27382335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35005405-C-T

27382364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35005430-T-G

27382414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35005473-C-T

27382521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35005585-G-T

27382661-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35005746-T-A

27382661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35005746-T-C

27382684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35005769-A-G

27385431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35005899-G-A

27385431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35005899-G-T

27385910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35006349-G-A

http://identifiers.org/hco/9/GRCh38#27386140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35006533-C-A

27386240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35006626-G-A

27387056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35007510-G-A

27387084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35007539-A-G

http://identifiers.org/hco/9/GRCh38#27387131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35007594-C-A

27387131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35007594-C-T

27387322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35008078-C-T

27387438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35008196-C-T

27387486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35008240-G-C

27387725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35008650-G-A

http://identifiers.org/hco/9/GRCh38#27387788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35008700-A-C

27387838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35008727-T-C

27387847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35008736-T-A

27387847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35008736-T-C

http://identifiers.org/hco/9/GRCh38#27387902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35008769-A-C

27387902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35008769-A-G

27387902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35008769-A-T

27387918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35008785-T-C

27387938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35008804-T-C

27390790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35010566-A-G

27390906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35010684-T-G

27390930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35010705-G-A

27390930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35010705-G-T

27391849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35011301-G-T

27391924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35011376-A-G

27392008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35011444-T-G

27392037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35011474-A-G

27392044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35011481-T-A

http://identifiers.org/hco/9/GRCh38#27392712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35011666-C-A

27392712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35011666-C-T

27392829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35011786-T-A

27392907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35011834-T-C

27392914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35011841-G-A

27392919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35011846-G-T

27392954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35011881-T-C

27393003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35011917-G-A

27393003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35011917-G-C

http://identifiers.org/hco/9/GRCh38#27393159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35012065-A-C

27393179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35012084-A-G

27393411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35012184-T-G

27393767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35012493-G-A

27393777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35012502-G-A

27394045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35012822-G-T

27394096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35012873-T-C

27394128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35012905-A-G

27394191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35012945-A-G

27394192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35012946-T-C

27394193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35012947-G-T

http://identifiers.org/hco/9/GRCh38#27394199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35012959-C-A

27394199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35012959-C-T

http://identifiers.org/hco/9/GRCh38#27394321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35013047-C-A

27394342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35013068-G-T

27394371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35013097-G-T

27395455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35014625-A-T

27395466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35014636-G-A

27395498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35014652-G-C

27396386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35016341-C-T

27396394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35016349-A-G

27396542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35016465-T-C

http://identifiers.org/hco/9/GRCh38#27396642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35016547-C-A

27396642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35016547-C-T

27396740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35016641-A-G

http://identifiers.org/hco/9/GRCh38#27396809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35016715-C-A

27396819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35016724-G-T

27396865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35016778-C-T

27397122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35017007-G-T

27397168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35017060-C-T

27397462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35017350-C-T

27397549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35017436-G-A

27397549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35017436-G-T

27397857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35017744-G-T

27397875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35017758-A-G

27398185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35018069-C-G

27398264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35018168-A-G

27398471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35018323-C-T

http://identifiers.org/hco/9/GRCh38#27398569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35018407-C-A

27398681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35018557-A-G

27398762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35018726-T-A

27398762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35018726-T-C

27398784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35018748-T-C

27399093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35019098-C-T

27399176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35019169-C-G

27399176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35019169-C-T

27399410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35019380-A-G

27399770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35019741-G-C

27401086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35020133-G-T

27401101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35020146-G-A

27401225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35020269-G-A

27401282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35020326-G-A

27401282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35020326-G-C

27401389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35020385-G-T

27401492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35020466-C-T

27401540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35020518-G-T

http://identifiers.org/hco/9/GRCh38#27401550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35020535-C-A

27401550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35020535-C-T

27401790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35020765-C-T

27401880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35020849-C-T

27401966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35020937-A-G

27402164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35021101-T-G

27402201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35021137-A-G

27402618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35021505-A-T

27402625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35021512-T-C

27402916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35021978-T-G

27402992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35022052-C-T

27403008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35022068-C-T

27403152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35022170-T-A

http://identifiers.org/hco/9/GRCh38#27407662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35022965-C-A

27407748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35023046-C-T

27407784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35023079-T-C

http://identifiers.org/hco/9/GRCh38#27407959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35023269-C-A

27408044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35023354-T-C

27408124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35023385-C-G

27408210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35023479-A-G

27408211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35023480-G-A

27408329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35023586-A-G

27408594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35023826-C-G

27408605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35023836-A-G

27408743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35023982-C-T

27408823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35024063-C-T

http://identifiers.org/hco/9/GRCh38#27409232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35024378-C-A

27409641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35025098-A-G

27409737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35025192-T-C

27409940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35025400-G-C

http://identifiers.org/hco/9/GRCh38#27410311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35025723-C-A

27410311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35025723-C-T

27410544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35026820-T-A

http://identifiers.org/hco/9/GRCh38#27410643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35026916-C-A

27410786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35027059-C-T

27410915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35027137-C-T

27410996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35027218-A-G

27411000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35027222-G-C

27411137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35027399-C-G

27411267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35027530-G-T

27411329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35027596-C-T

27411433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35027698-C-T

27411444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35027709-C-T

27411494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35027750-C-T

27411679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35027966-A-G

27411824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35028067-C-T

http://identifiers.org/hco/9/GRCh38#27411927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35028170-A-C

27411993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35028235-T-C

27412117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35028365-G-A

http://identifiers.org/hco/9/GRCh38#27412155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35028395-C-A

27413089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35030312-T-C

http://identifiers.org/hco/9/GRCh38#27413170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35030370-A-C

27413170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35030370-A-G

27413247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35030473-G-A

27413247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35030473-G-C

27413299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35030529-C-G

27413374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35030586-G-A

http://identifiers.org/hco/9/GRCh38#27413433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35030639-A-C

27413575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35030760-G-A

27413575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35030760-G-C

27413579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35030771-C-T

27413587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35030779-G-T

http://identifiers.org/hco/9/GRCh38#27413803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35030995-A-C

27414042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35031226-A-G

27414064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35031248-T-A

http://identifiers.org/hco/9/GRCh38#27414136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35031320-C-A

27414136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35031320-C-G

27414210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35031394-C-T

http://identifiers.org/hco/9/GRCh38#27414299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35031468-A-C

27414301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35031470-T-C

27414451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35031591-T-C

27414633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35031758-C-T

27414705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35031828-C-G

27414705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35031828-C-T

27414761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35031864-G-C

27414768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35031871-G-A

http://identifiers.org/hco/9/GRCh38#27414801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35031904-A-C

27415259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35032059-C-T

27415423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35032204-T-A

27415445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35032226-G-A

27415733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35032502-G-A

27415803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35032544-T-C

27416198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35033957-A-G

27416262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35033999-A-G

27416268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35034005-T-C

27416419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35034170-G-C

http://identifiers.org/hco/9/GRCh38#27416502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35034238-C-A

27417539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35034575-G-A

27417641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35034664-C-T

27417642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35034665-T-C

27417693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35034717-T-C

27422210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35036044-T-C

27422596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35036400-C-T

http://identifiers.org/hco/9/GRCh38#27422657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35036461-A-C

27422660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35036480-C-T

27422782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35036599-A-T

http://identifiers.org/hco/9/GRCh38#27422784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35036601-C-A

http://identifiers.org/hco/9/GRCh38#27422827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35036629-C-A

27423051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35037002-A-G

27423063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35037014-A-T

27423276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35037239-G-C

27423276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35037239-G-T

http://identifiers.org/hco/9/GRCh38#27423552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35037511-A-C

27426920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35037701-T-C

27427121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35037880-T-A

27427184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35037947-A-T

27427267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35038016-T-C

27427311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35038060-C-T

27427382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35038121-T-C

27427436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35038175-C-T

27427687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35038408-C-T

27427918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35039632-A-G

27428010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35039719-C-T

27428996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35040661-G-A

27429150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35040802-C-G

http://identifiers.org/hco/9/GRCh38#27429828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35042035-A-C

27429838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35042045-G-A

27429886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35042117-C-G

27429909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35042137-C-G

27429958-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35042176-C-G

27430013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35042226-A-T

27430060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35042273-C-T

27430793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35049112-T-C

27430947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35049269-C-T

27430988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35049308-G-T

27431028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35049347-T-C

http://identifiers.org/hco/9/GRCh38#27431218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35049573-C-A

27431279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35049644-T-C

27431284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35049649-T-A

27431408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35049765-T-A

27431448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35049799-A-T

27431520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35049871-T-C

27432260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35050682-C-T

27433034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35051586-C-T

http://identifiers.org/hco/9/GRCh38#27433097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35051613-C-A

27433097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35051613-C-T

27433323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35051692-C-T

27433425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35051787-C-T

27433563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35052235-T-C

27433589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35052261-A-G

27433730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35052398-A-G

27433746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35052414-G-T

27433861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35052524-T-C

27433926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35052587-G-A

27433981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35052637-G-C

27434072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35052720-T-C

27434072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35052720-T-G

27434205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35052846-T-G

27434396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35052979-C-T

http://identifiers.org/hco/9/GRCh38#27434554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35053694-A-C

27434885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35054014-T-C

27434925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35054054-T-C

27435135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35054211-G-T

27435231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35054289-T-G

27435258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35054318-G-A

27435268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35054328-T-A

27435268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35054328-T-C

27435603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35054463-A-G

27436062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35054735-C-G

27436230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35054883-A-G

27436355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35055014-G-A

27436444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35055088-C-T

http://identifiers.org/hco/9/GRCh38#27436496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#35055139-C-A

27436496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35055139-C-T

http://identifiers.org/hco/9/GRCh38#27436497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#35055140-A-C

27436497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35055140-A-G

27436498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35055141-T-C

27436511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35055154-C-G

27436590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35055221-T-G

27436857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35057327-G-C

http://identifiers.org/hco/9/GRCh38#27437006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35057447-C-A

27437006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35057447-C-G

27437015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35057456-G-A

27437015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35057456-G-T

27437039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35057468-T-G

27437088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35057517-A-G

27437236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35057665-T-C

27437480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35057885-T-C

27437587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35057981-G-A

27437702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35058066-G-A

27437726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35058083-C-T

27438419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35058228-G-A

27438420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35058229-A-T

27438421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35058230-G-C

http://identifiers.org/hco/9/GRCh38#27438517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35058479-C-A

27438545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35058507-C-T

http://identifiers.org/hco/9/GRCh38#27438622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35058582-C-A

27438669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35058628-C-T

27438951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35058850-G-A

27438979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35058876-G-C

27439754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35059560-T-C

http://identifiers.org/hco/9/GRCh38#27439858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35060034-C-A

27439858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35060034-C-T

27440004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35060144-C-G

27440215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35060350-G-C

27440394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35060508-C-T

http://identifiers.org/hco/9/GRCh38#27440403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35060517-C-A

27440403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35060517-C-T

27440683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35060802-G-A

27440708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35060827-T-G

27442998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35061246-G-A

27443138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35061385-C-T

http://identifiers.org/hco/9/GRCh38#27443503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35061684-C-A

27443784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35061956-A-G

27443787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35061961-C-G

27443820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35061997-C-T

27443879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35062054-G-A

http://identifiers.org/hco/9/GRCh38#27444347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35062280-C-A

27444347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35062280-C-G

27444402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35062335-G-A

27444402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35062335-G-T

27444485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35062415-C-T

27444489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35062419-T-C

27445171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35063211-G-A

27445186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35063224-A-T

27445608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35063569-T-C

27445650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35063610-G-A

27445946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35063880-G-A

27446089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35063985-G-A

27446107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35064003-A-G

27446219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35064263-A-T

http://identifiers.org/hco/9/GRCh38#27446370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35064406-C-A

27446423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35064432-T-C

27446641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35064610-C-G

27446719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35064691-G-A

http://identifiers.org/hco/9/GRCh38#27446744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35064717-C-A

27447003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35064913-T-C

27447004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35064914-G-A

27447004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35064914-G-T

27447059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35064966-G-A

27447059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35064966-G-C

27447059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35064966-G-T

27447169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35065049-G-A

27447221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35065100-G-A

27447329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35065198-T-A

27447523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35065378-G-C

http://identifiers.org/hco/9/GRCh38#27447886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35065723-C-A

27447886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35065723-C-T

27448045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35065914-T-G

27448105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35065959-C-T

27448173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35066027-C-T

27448193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35066062-G-T

27448259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35066120-T-C

27449012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35066525-G-A

27449285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35066991-C-T

27449351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067084-G-T

27449459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067200-G-A

27449492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067232-G-A

27449521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067261-C-T

27449561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067300-C-T

http://identifiers.org/hco/9/GRCh38#27449835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35067532-A-C

27449915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067609-C-T

27449926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067612-C-G

27449926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067612-C-T

27449938-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067624-A-T

27449942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067628-C-T

27450013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067666-T-G

27450043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067681-C-T

27450154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067765-G-C

27450154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067765-G-T

27450267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35067841-T-C

27450460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35068032-A-T

http://identifiers.org/hco/9/GRCh38#27450574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35068138-C-A

27450689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35068201-T-C

27450732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35068237-G-A

27450732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35068237-G-C

27450757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35068257-G-A

27450850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35068319-G-A

27450850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35068319-G-T

27450879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35068362-T-C

http://identifiers.org/hco/9/GRCh38#27450912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35068394-A-C

27451195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35068669-G-A

27451356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35068823-A-G

27451604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35069062-C-T

27451729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35069188-C-T

27451875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35069346-G-T

27451908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35069378-G-A

27451920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35069390-G-C

27451979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35069448-C-G

27452071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35069547-G-C

27453307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35082050-T-A

27453308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35082051-C-T

27453330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35082078-G-A

27453330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35082078-G-C

27453356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35082102-G-A

27453975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35082600-A-G

27454078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35082709-G-A

27454078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35082709-G-C

27454195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35082811-C-T

27454320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35082949-A-G

27454359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35082981-G-A

http://identifiers.org/hco/9/GRCh38#27454376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35082998-A-C

27454437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35083062-T-G

27454587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35083198-T-C

27454664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35083267-T-A

27454699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35083301-A-G

27454703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35083305-T-C

http://identifiers.org/hco/9/GRCh38#27454768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35083370-C-A

27454768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35083370-C-G

27454768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35083370-C-T

27454800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35083403-G-T

27454854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35083453-C-G

27455027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35083613-T-A

27455027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35083613-T-G

27455254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35083891-C-T

27455263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35083900-A-G

27455269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35083906-G-C

27455342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: 35083979-C-G

27455342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: 35083979-C-T

27455343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: 35083980-G-A

27455343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35083980-G-T

http://identifiers.org/hco/9/GRCh38#27455355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35083992-C-A

27455364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: 35084001-G-A

27455394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: 35084031-C-G

http://identifiers.org/hco/9/GRCh38#27455396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35084033-C-A

27455396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: 35084033-C-T

27455421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35084058-G-A

27455429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: 35084066-C-T

27455431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35084068-C-G

27455431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35084068-C-T

27455443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35084080-T-C

27455454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: 35084091-G-A

27455454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: 35084091-G-C

27455473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: 35084110-C-G

27455473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35084110-C-T

27455474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: 35084111-T-C

27455479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35084116-G-T

27455482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35084119-A-G

27455485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35084122-T-C

http://identifiers.org/hco/9/GRCh38#27455504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35084141-C-A

27455504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: 35084141-C-T

27455505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: stop gained
orthologous variants: 35084142-G-A

27455505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35084142-G-T

http://identifiers.org/hco/9/GRCh38#27455541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35084178-C-A

27455542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: synonymous variant
orthologous variants: 35084179-T-A

27455542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: missense variant
orthologous variants: 35084179-T-C

27455631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5 prime UTR variant
orthologous variants: 35084268-G-A

27455633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5 prime UTR variant
orthologous variants: 35084270-G-A

27455641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5 prime UTR variant
orthologous variants: 35084278-C-G

27455641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5 prime UTR variant
orthologous variants: 35084278-C-T

http://identifiers.org/hco/9/GRCh38#27455677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35084314-C-A

27455684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5 prime UTR variant
orthologous variants: 35084321-G-A

27455684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5 prime UTR variant
orthologous variants: 35084321-G-C

27455702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5 prime UTR variant
orthologous variants: 35084343-T-C

http://identifiers.org/hco/9/GRCh38#27455708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35084349-C-A

27455708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5 prime UTR variant
orthologous variants: 35084349-C-G

27455708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5 prime UTR variant
orthologous variants: 35084349-C-T

27455736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5 prime UTR variant
orthologous variants: 35084377-C-G

27455768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35084409-G-A

27455768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35084409-G-T

27455878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35084524-G-A

27455878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35084524-G-C

27455878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35084524-G-T

27455889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35084535-G-A

27455889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35084535-G-T

http://identifiers.org/hco/9/GRCh38#27455928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35084576-A-C

27456128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35084711-G-C

27456212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35084781-T-C

27456268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35084817-T-C

27456378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35084958-G-A

27456447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35085028-A-T

27456530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35085142-G-C

27456605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35085221-G-A

27456853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35085470-T-G

27456914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35085538-C-T

27457018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35085632-G-A

27457018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35085632-G-T

http://identifiers.org/hco/9/GRCh38#27457332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35085949-C-A

27457332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35085949-C-T

http://identifiers.org/hco/9/GRCh38#27457343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35085960-A-C

27457568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35086257-C-T

27457712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35086386-G-T

27457815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35086485-T-C

27457911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35086656-A-G

27458110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35086897-C-T

27459019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35087918-C-G

27459113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35088001-C-T

http://identifiers.org/hco/9/GRCh38#27459618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35088694-C-A

27459618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35088694-C-G

27459618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35088694-C-T

27459816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35088938-C-T

27459986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35089141-T-C

http://identifiers.org/hco/9/GRCh38#27460049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35089206-A-C

27460565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35089689-C-T

27460672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35089781-A-G

27460845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35089969-G-C

27460956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35090071-G-A

27460989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35090121-G-C

http://identifiers.org/hco/9/GRCh38#27461038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35090169-C-A

27461041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35090172-C-T

27461190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35090315-C-T

27461266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35091054-G-A

27461266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35091054-G-C

27461320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35091109-C-G

27461320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35091109-C-T

http://identifiers.org/hco/9/GRCh38#27461336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35091125-A-C

27461358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35091133-G-A

27461633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35091382-C-T

27461761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35091508-T-C

27462096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35091847-C-T

27462263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35092142-T-C

27462263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35092142-T-G

27462504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35092511-C-T

27462886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35092912-T-C

27462889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35092915-G-A

27463214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35093326-A-G

27463244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35093367-C-T

27463245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35093368-T-C

27463750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35093711-C-T

27463759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35093735-G-A

27464225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35094225-G-A

27464455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35094647-C-T

http://identifiers.org/hco/9/GRCh38#27464486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35094690-A-C

27464489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35094693-A-G

27464554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35094769-T-C

27464588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35094805-G-A

http://identifiers.org/hco/9/GRCh38#27467586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35095476-A-C

27467591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35095481-T-C

http://identifiers.org/hco/9/GRCh38#27467620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35095510-A-C

27467693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35095585-A-T

27467716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35095602-T-A

27467716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35095602-T-C

27467716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35095602-T-G

27467978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35096260-C-G

27468049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35096336-A-G

27468049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35096336-A-T

27468123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35096408-T-C

27468129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35096414-C-T

27468380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35096644-T-G

http://identifiers.org/hco/9/GRCh38#27468529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35096753-C-A

27468529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35096753-C-T

27468583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35096824-T-C

27468871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35097076-T-C

27469494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35098011-C-T

27469627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35098126-C-T

http://identifiers.org/hco/9/GRCh38#27470284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35098434-A-C

http://identifiers.org/hco/9/GRCh38#27470345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35098473-C-A

27470345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35098473-C-T

27470586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35098660-A-G

http://identifiers.org/hco/9/GRCh38#27470661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35098730-C-A

27470661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35098730-C-G

27470789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35098848-C-G

27470861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35098921-C-G

27470919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35098958-T-C

27470944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35098977-G-T

27470961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35098994-G-A

27471068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35099098-G-A

http://identifiers.org/hco/9/GRCh38#27471099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35099127-C-A

27471136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35099165-A-G

27471389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35099396-G-C

27471389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35099396-G-T

27471430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35099447-T-C

http://identifiers.org/hco/9/GRCh38#27471443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35099460-C-A

27471443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35099460-C-T

27471444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35099463-G-A

27471884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35099874-G-A

27472081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35100312-T-C

http://identifiers.org/hco/9/GRCh38#27472408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35100481-C-A

27472408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35100481-C-G

27472408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35100481-C-T

27472426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35100499-T-A

http://identifiers.org/hco/9/GRCh38#27472464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35100536-C-A

http://identifiers.org/hco/9/GRCh38#27472658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35100918-C-A

http://identifiers.org/hco/9/GRCh38#27472668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35100928-C-A

27472668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35100928-C-T

http://identifiers.org/hco/9/GRCh38#27472670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35100930-C-A

27472674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35100934-A-G

27472674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35100934-A-T

27472905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35101107-G-A

27472946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35101160-T-C

27473090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35101312-C-T

27473172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35101396-C-G

27473258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35101481-G-A

27473331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 35101557-G-A

27474306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35102106-T-C

27474758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35102539-T-C

27475084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35103257-C-T

27475149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35103320-T-G

27475221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35103388-G-A

27475318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35103477-C-T

27475319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35103478-G-A

27475370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35103528-A-T

27475590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35103728-T-A

27475687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35103907-C-T

27475811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35104220-C-G

27475958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35104353-T-C

http://identifiers.org/hco/9/GRCh38#27475972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35104367-C-A

27475972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35104367-C-T

27476000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35104394-C-T

27476037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35104431-T-C

27476495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35104849-T-A

27476795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35105098-T-C

27476902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35105204-A-G

27476946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35105249-C-G

27476946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35105249-C-T

27476998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35105294-C-T

27477239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35105524-C-G

http://identifiers.org/hco/9/GRCh38#27477338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35105645-A-C

27477474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35105743-T-C

27477552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35105808-C-T

27477714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35105979-T-C

27477851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35106103-C-T

27477907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35106158-T-C

27478038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35106275-T-G

http://identifiers.org/hco/9/GRCh38#27478189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35106439-C-A

27478390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35106646-G-A

27478390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35106646-G-T

27482049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35109139-C-T

27482273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35109348-T-C

27482349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35109415-A-T

27482448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35109512-G-A

27482448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35109512-G-C

27482889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35109685-A-G

27483516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35112059-C-T

27483725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35112318-C-T

27483814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35112391-T-C

27483833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35112410-G-C

27484048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35112648-G-A

27484090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35112692-A-G

http://identifiers.org/hco/9/GRCh38#27484116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35112721-C-A

27484116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35112721-C-G

27484132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35112737-C-T

27484253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35112838-C-T

27484376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35112939-A-G

27484495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35113043-T-G

27484607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35113300-G-A

27485032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35113788-T-C

27485035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35113791-A-G

27485108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35113856-T-C

27485113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35113861-A-G

27485299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 35114231-T-C

27485480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35114417-C-T

27485701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35114514-A-G

27485743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35114560-C-G

27485795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35114612-G-C

27485824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35114634-T-A

27485882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35114691-T-C

27485894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35114703-G-T

27485907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35114714-C-G

27489168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35115856-C-T

27489420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35116077-G-A

27489551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35116193-T-C

27489726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35116366-A-T

http://identifiers.org/hco/9/GRCh38#27490009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35118811-C-A

27490067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35118872-C-T

27490228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35119056-A-G

27490327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35119133-G-A

27490429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35119235-A-G

27490446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35119252-G-C

27490479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35119280-G-T

27490744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35119476-C-G

27490943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35119925-G-C

27490965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35119947-G-A

27490995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35119975-T-A

27490995-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35119975-T-G

27490998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35119978-G-T

27491003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35119983-T-A

27491006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35119986-A-G

27491351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35120312-A-G

27491355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35120316-T-A

27491475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35120383-T-C

27491968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35120597-G-A

27491968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35120597-G-T

27492012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35120640-C-T

27492034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35120662-T-C

http://identifiers.org/hco/9/GRCh38#27492463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35121060-C-A

http://identifiers.org/hco/9/GRCh38#27492502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35121084-A-C

27492502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35121084-A-G

27492516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35121098-C-G

27492580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35121156-T-C

27492594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35121170-A-G

27492595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35121171-A-G

27492712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35121288-T-C

27492791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35121367-G-A

27492805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35121381-G-A

http://identifiers.org/hco/9/GRCh38#27493050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35121625-C-A

27496329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35123490-T-G

27496925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35124081-T-C

27496971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35124127-C-T

27497006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35124173-C-T

27497133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35124375-A-T

27497194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35124435-G-A

27497237-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35124478-T-A

27497264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35124505-A-G

27497264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35124505-A-T

27497277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35124518-G-A

http://identifiers.org/hco/9/GRCh38#27497666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35125007-A-C

27497869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35125217-A-G

27497970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35125316-T-G

27498091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35125442-T-C

http://identifiers.org/hco/9/GRCh38#27498107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35125459-C-A

27498107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35125459-C-G

27498107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35125459-C-T

27498141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35125495-C-T

27498186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35125539-C-T

27498263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35125614-C-T

27498346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35125697-T-C

27498429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35125775-G-A

27498693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35126015-A-G

http://identifiers.org/hco/9/GRCh38#27499154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35126785-A-C

27499296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35126925-A-T

http://identifiers.org/hco/9/GRCh38#27502564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35127486-C-A

27502620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35127550-G-A

27502656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35127602-C-T

27502694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35127637-A-G

27502774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35127699-C-G

27503500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35128376-G-A

http://identifiers.org/hco/9/GRCh38#27503722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35128592-C-A

27503722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35128592-C-G

27503837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35128730-A-G

27504032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35128909-A-G

27504315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35129175-A-T

27505317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35130072-C-T

27505451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35130199-G-A

27505573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35130314-G-A

27505616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35130357-A-G

27505703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35130441-T-C

http://identifiers.org/hco/9/GRCh38#27506310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35131032-C-A

27506403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35131090-C-T

27506457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35131169-C-T

27506472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35131184-T-A

27507012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35131257-T-A

27507104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35131341-C-G

27507156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35131393-A-G

27507186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35131419-C-T

27507320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35131540-G-A

27507591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35131695-T-C

27508630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35135103-C-T

27508836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35135311-G-A

27508952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35135436-G-T

27508959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35135441-T-C

27508978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35135460-G-A

27509050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35135516-A-G

27509190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35135649-A-G

27511003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35138422-G-A

27511061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35138499-G-A

27511079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35138506-A-G

27511103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35138528-G-A

27511587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35140045-T-C

27511587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35140045-T-G

27511605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35140060-G-A

http://identifiers.org/hco/9/GRCh38#27511632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35140085-A-C

27511886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35140317-T-A

http://identifiers.org/hco/9/GRCh38#27511977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35140385-C-A

27512016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35140421-G-A

27512039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35140446-G-A

27512062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35140469-C-T

27512487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35141127-A-G

27512528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35141160-T-C

27512657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35141282-G-T

27512939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35142160-A-G

27512995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35142221-A-G

27513117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35142344-T-C

27513267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35142476-C-G

27513308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35142521-C-T

27513368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35142570-T-C

27513388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35142587-G-A

http://identifiers.org/hco/9/GRCh38#27513425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35142625-C-A

27513658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35142855-G-A

27513666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35142864-C-T

27513816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35142997-G-C

27514324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35143466-C-T

http://identifiers.org/hco/9/GRCh38#27514339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35143481-C-A

27514339-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35143481-C-G

27514723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35143796-T-A

27514849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35143909-G-A

27514985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35144061-T-C

27515070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35144141-A-G

27515275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35144375-T-G

27515435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35144550-A-T

27517844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35145175-T-C

27518171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35145966-T-C

27518229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35145994-T-G

27518254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35146020-G-A

27518344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35146104-G-A

27518344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35146104-G-C

27518344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35146104-G-T

27518418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35146174-C-T

27518517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35146249-G-A

27518556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35146288-C-T

27518670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35146401-C-G

27518670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35146401-C-T

http://identifiers.org/hco/9/GRCh38#27519150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35146823-C-A

27519150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35146823-C-T

http://identifiers.org/hco/9/GRCh38#27519357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35147008-A-C

27519357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147008-A-G

27519363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147014-T-C

27519366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147017-C-T

27519551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147201-G-A

27519639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147286-T-C

27519665-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147317-A-T

27519697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147347-C-G

27519742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147407-G-A

27519789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147451-A-G

27519810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147464-A-T

27519822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147474-G-T

27519889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147512-A-T

27519963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147551-G-T

http://identifiers.org/hco/9/GRCh38#27519969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35147557-C-A

27519969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147557-C-T

27520027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147600-T-G

27520032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35147605-A-G

27520306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35148061-G-A

27520510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35148259-A-G

27520615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35148365-T-C

27520752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35148466-G-A

27520927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35148649-T-G

27521010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35148733-T-A

27521294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35148951-G-C

27521600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35149244-T-A

27521600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35149244-T-C

27521614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35149262-G-A

27521627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35149275-G-C

27521723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35149358-T-C

27522509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35150082-T-C

27522682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35150209-G-A

27522918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35150474-T-C

27523053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35150597-T-C

27523103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35150647-T-C

27523137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35150690-A-G

http://identifiers.org/hco/9/GRCh38#27523549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35151066-A-C

27523667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35151174-A-G

27523762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35151601-T-C

http://identifiers.org/hco/9/GRCh38#27524176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35151951-C-A

27524176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35151951-C-G

27524176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35151951-C-T

27524345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 35152063-C-G

27524345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 35152063-C-T

27524368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant
orthologous variants: 35152087-G-A

27524504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 35152211-T-C

27524578-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant
orthologous variants: 35152285-G-C

27524785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, stop_gained
orthologous variants: 35152467-C-G

27524912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 35152592-A-G

http://identifiers.org/hco/9/GRCh38#27524984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35152658-C-A

27524984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35152658-C-G

27525049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35152705-G-A

27525049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35152705-G-T

http://identifiers.org/hco/9/GRCh38#27525075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35152735-C-A

27525075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35152735-C-T

27525092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35152784-T-C

http://identifiers.org/hco/9/GRCh38#27525264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35152957-A-C

27525264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35152957-A-G

27525298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35152991-G-A

27525431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35153116-G-T

http://identifiers.org/hco/9/GRCh38#27525894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35153697-C-A

27525933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35153724-T-C

27525933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35153724-T-G

http://identifiers.org/hco/9/GRCh38#27525991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35153771-A-C

http://identifiers.org/hco/9/GRCh38#27525993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35153773-C-A

http://identifiers.org/hco/9/GRCh38#27526046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35153828-C-A

27526046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35153828-C-T

http://identifiers.org/hco/9/GRCh38#27526111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35153849-C-A

27526111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35153849-C-T

27526112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35153850-A-G

27526112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35153850-A-T

http://identifiers.org/hco/9/GRCh38#27526153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35153894-C-A

27526153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35153894-C-T

http://identifiers.org/hco/9/GRCh38#27526174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35153914-C-A

27526174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35153914-C-T

27526181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35153921-C-T

27526316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35154055-A-G

27526328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35154067-G-C

27526328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35154067-G-T

27526350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35154093-A-G

27526400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 35154129-G-T

27526535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35154261-T-C

27527013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35154824-A-T

27527021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35154832-C-T

27527340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35155080-G-A

27527340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35155080-G-T

27527383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35155121-G-T

27527752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35155533-G-A

27527799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35155569-G-T

http://identifiers.org/hco/9/GRCh38#27528110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35155886-C-A

27528115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35155891-C-G

27528150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35155926-C-T

http://identifiers.org/hco/9/GRCh38#27528241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35156013-C-A

27528291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35156056-T-C

http://identifiers.org/hco/9/GRCh38#27528305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35156070-C-A

27528305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35156070-C-G

http://identifiers.org/hco/9/GRCh38#27528316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35156080-C-A

27528522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 35156259-A-G

http://identifiers.org/hco/9/GRCh38#27528607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35156344-C-A

27528607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant
orthologous variants: 35156344-C-T

27528756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35156506-G-C

27528757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: 35156507-G-A

http://identifiers.org/hco/9/GRCh38#27528844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#35156589-C-A

27528880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35156634-T-G

27528934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron variant
orthologous variants: 35156681-G-A

27529024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 35156766-C-T

27529067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 35156810-T-G

http://identifiers.org/hco/9/GRCh38#27529240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#35156976-C-A

27529253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35156982-T-G

27529427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35157147-G-A

27529427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35157147-G-T

http://identifiers.org/hco/9/GRCh38#27529429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#35157149-C-A

27529466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 35157171-C-T

http://identifiers.org/hco/9/GRCh38#27529479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#35157182-C-A

27529479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35157182-C-T

27529486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35157189-G-A

27529486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35157189-G-T

27529487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35157190-G-A

27529487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35157190-G-T

http://identifiers.org/hco/9/GRCh38#27529600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35157298-C-A

27529600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35157298-C-T

http://identifiers.org/hco/9/GRCh38#27529611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#35157309-C-A

27529611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35157309-C-T

http://identifiers.org/hco/9/GRCh38#27529656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/4/GRCm39#35157357-C-A

27529767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23825
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35157430-A-G