47856728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42832287-C-T

47857011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42832014-T-C

47857078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42831945-A-G

http://identifiers.org/hco/6/GRCh38#47857262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42831751-A-C

47857342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42831677-T-C

http://identifiers.org/hco/6/GRCh38#47857445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42831590-C-A

47857810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42831285-G-A

47857810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42831285-G-T

47858008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42831123-T-A

47858229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42830902-C-T

47858299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42830832-C-T

47858347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42830784-C-T

47858352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42830778-A-G

47858366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42830764-T-C

47858409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42830721-A-G

http://identifiers.org/hco/6/GRCh38#47858656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42830470-C-A

47858656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42830470-C-T

47858841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42830304-T-A

47859087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42830072-A-G

47859159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42830000-A-G

http://identifiers.org/hco/6/GRCh38#47859254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42829914-A-C

47859291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42829877-G-A

47859291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42829877-G-C

47859313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42829855-A-G

47859377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42829792-G-A

47859399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42829771-G-A

47859399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42829771-G-C

47860003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42829591-C-T

47860072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42829537-A-G

47860072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42829537-A-T

47860499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42829163-T-C

47860531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42829131-G-A

47860560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42829103-T-C

47860853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42828821-T-C

47862355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42828610-C-T

47862448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42828525-C-G

47862524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42828466-T-A

http://identifiers.org/hco/6/GRCh38#47862543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42828449-A-C

47862543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42828449-A-G

47862657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42828314-T-C

http://identifiers.org/hco/6/GRCh38#47862662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42828309-C-A

47862789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42828214-A-T

47862843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42828156-T-G

47862987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42828053-T-C

47863044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42827996-A-G

47863074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42827968-T-C

47863174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42827878-G-A

47863236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42827743-T-A

47863431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42827567-G-A

47863491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42827512-G-C

47863554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42827451-A-G

47863770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42827290-G-C

47865901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42827079-G-C

http://identifiers.org/hco/6/GRCh38#47865940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42827043-A-C

47866058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42826943-A-G

47866203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42826629-A-G

47866469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42826371-C-T

47866501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42826339-T-C

47866570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42826272-G-A

47866590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42826252-G-A

http://identifiers.org/hco/6/GRCh38#47866727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42826177-A-C

47866985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42825705-C-T

47867033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42825657-G-A

47867033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42825657-G-T

http://identifiers.org/hco/6/GRCh38#47867071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42825620-C-A

47867071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42825620-C-T

47867153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42825581-A-G

47867175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42825560-T-C

47867244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42825491-A-T

47867255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42825476-G-A

47867257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42825474-C-T

http://identifiers.org/hco/6/GRCh38#47867322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42825413-C-A

47867569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42825194-T-C

http://identifiers.org/hco/6/GRCh38#47867608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42825158-C-A

47867743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42825072-G-T

http://identifiers.org/hco/6/GRCh38#47867784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42825031-C-A

47867794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42825021-C-T

47867809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42825018-A-G

47867828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824994-T-C

47867878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824951-G-A

47867958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824885-T-A

47868055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824810-T-C

47868174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824726-T-A

47868212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824718-T-C

47868250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824681-C-T

http://identifiers.org/hco/6/GRCh38#47868354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42824581-C-A

47868861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824476-T-C

http://identifiers.org/hco/6/GRCh38#47868935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42824402-C-A

47869232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824131-G-A

47869248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824119-T-C

47869272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824095-A-G

47869283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824084-A-G

47869323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824048-G-A

47869364-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42824018-T-A

http://identifiers.org/hco/6/GRCh38#47870132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42822652-A-C

47870147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42822637-A-G

47870257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42822534-T-C

http://identifiers.org/hco/6/GRCh38#47871128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42821679-C-A

47871128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42821679-C-T

47871319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42821501-A-G

47871319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42821501-A-T

47871419-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42821414-T-A

47871419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42821414-T-C

47871541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42821270-T-G

47871580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42821230-G-C

47871583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42821227-G-A

47871583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42821227-G-C

47871625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42821185-A-G

47871799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42821041-G-A

47872021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42820842-G-A

47872133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42820732-A-G

47872331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42820533-T-A

47872394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42820469-A-G

47872482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42820392-C-G

47872482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42820392-C-T

47872914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42819962-C-T

47872932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42819940-A-T

47873241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42819689-T-C

http://identifiers.org/hco/6/GRCh38#47873431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42819485-C-A

47873431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42819485-C-T

47873439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42819477-G-C

47873811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42819122-G-A

47873940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42818993-A-G

47874029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42818906-A-G

47874097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42818845-C-T

47874110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42818832-T-A

47874110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42818832-T-C

http://identifiers.org/hco/6/GRCh38#47874887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42818061-C-A

47874888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42818060-T-G

47874901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42818056-T-C

47874932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42818039-T-C

47875031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42817967-C-T

47875041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42817957-G-C

http://identifiers.org/hco/6/GRCh38#47875244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42817762-C-A

47875245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42817761-T-A

http://identifiers.org/hco/6/GRCh38#47875247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42817759-C-A

47875297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42817715-C-T

47875647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42817367-G-A

47875665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42817350-G-T

47876026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42817006-A-G

47876423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42816678-G-C

47876585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42816578-G-A

47876651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42816505-A-G

47876940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42816141-A-G

47876999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42816097-G-T

47877215-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42815889-T-A

47877310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42815780-C-T

47877574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3 prime UTR variant
orthologous variants: 42815513-C-G

47878748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: missense variant
orthologous variants: 42814359-A-G

47878757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: missense variant
orthologous variants: 42814350-T-C

47878868-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: missense variant
orthologous variants: 42814239-A-T

47879039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: missense variant
orthologous variants: 42814068-T-C

47879163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: missense variant
orthologous variants: 42813944-T-C

47879330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: missense variant
orthologous variants: 42813777-G-A

47879540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: missense variant
orthologous variants: 42813567-T-C

47879981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42813126-C-T

http://identifiers.org/hco/6/GRCh38#47880202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42812925-A-C

47880579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42811283-G-A

47880646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42811222-G-C

47880715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42811152-T-A

47880815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42811027-G-A

47880837-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42811005-A-T

47880948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42810903-A-G

47881089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42810764-G-A

47881122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42810732-C-T

47881358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42810493-C-T

47881364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42810487-C-G

47881372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42810479-C-T

47881392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42810461-G-C

47881781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42810116-A-G

http://identifiers.org/hco/6/GRCh38#47882051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42809867-C-A

47882051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42809867-C-T

47882312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42809619-A-G

47882480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42809457-A-G

47882545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42809393-T-C

47882610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42809331-T-C

47882743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42809224-T-G

47882766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42809199-T-A

47882766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42809199-T-C

47882766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42809199-T-G

47882928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42809049-T-C

47883008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42808749-G-A

47883008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42808749-G-T

47883048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42808711-T-G

47883166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42808600-A-G

47883200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42808570-C-T

47883328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42808432-T-C

http://identifiers.org/hco/6/GRCh38#47883365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42808394-C-A

47883786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42807509-G-A

47883786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42807509-G-T

47884006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42807307-A-G

47884150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42807216-A-G

47884582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42806831-C-G

47884999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42806032-T-C

47885275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42805771-T-C

47885613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42804575-G-A

47885613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42804575-G-C

47886193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42804221-C-T

47886238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42804177-T-G

47886319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42804150-G-T

47890742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42795757-T-A

47891381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42795119-G-C

http://identifiers.org/hco/6/GRCh38#47891425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42795076-C-A

47891425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42795076-C-G

47891577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42794941-G-T

47891680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42794861-C-T

47891703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42794835-A-G

47891787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42794756-A-G

47891912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42794637-T-A

47891924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42794626-G-C

47891975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42794574-T-G

47892418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42794108-C-T

47892811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42793712-G-A

http://identifiers.org/hco/6/GRCh38#47892904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42791714-C-A

47892904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42791714-C-G

47892908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42791710-A-T

47901442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42789427-G-A

47901442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42789427-G-C

47901442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42789427-G-T

47901452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42789417-T-A

http://identifiers.org/hco/6/GRCh38#47901693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42789174-C-A

47901693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42789174-C-T

47901705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42789168-G-A

47901705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42789168-G-T

47901779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42789123-A-G

47901798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42789104-T-A

47901801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42789101-A-G

http://identifiers.org/hco/6/GRCh38#47901804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42789098-C-A

47901804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42789098-C-T

47901836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42789067-G-T

http://identifiers.org/hco/6/GRCh38#47901940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42788964-A-C

47902672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42787250-G-A

47902685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42787239-T-C

47902703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42787221-C-T

47902717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42787197-T-A

47902858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42787060-T-A

47902858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42787060-T-C

47902881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42787034-A-G

http://identifiers.org/hco/6/GRCh38#47902931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42786980-C-A

47902933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42786978-C-T

47908667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42784795-C-T

47908805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42784658-C-T

47909026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42784418-G-T

47909086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42784358-G-C

47913430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42779923-G-A

http://identifiers.org/hco/6/GRCh38#47913488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42779868-A-C

47913488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42779868-A-G

47913545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42779811-T-A

47913548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42779808-T-G

47913643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42779718-G-C

47913688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42779674-G-A

47913688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42779674-G-C

47914053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42777679-T-C

47914149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42777585-T-G

47914395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42777374-T-A

47914549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42777254-A-G

47915176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42776063-G-T

47915421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42775834-C-T

47915451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42775803-G-A

47915511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42775742-G-T

47915704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42775594-C-T

47915722-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42775576-T-G

http://identifiers.org/hco/6/GRCh38#47915847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42775455-C-A

47915847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42775455-C-G

47915894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42775411-G-A

47915894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42775411-G-C

47915955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42775361-C-G

47915955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42775361-C-T

47916536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42773668-C-T

http://identifiers.org/hco/6/GRCh38#47916624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42773609-C-A

47916801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42773479-A-T

http://identifiers.org/hco/6/GRCh38#47916838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42773448-A-C

47916964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42773324-T-C

47917183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42773211-T-C

47917183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42773211-T-G

47917204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42773189-T-C

47917307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42773097-C-T

47917680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42772763-A-G

47917770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42772681-A-T

47918204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42772290-A-T

47918275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42772201-T-G

47918388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42772081-G-A

47918814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42771700-C-T

47918833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42771681-G-A

http://identifiers.org/hco/6/GRCh38#47918936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42771611-C-A

47918936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42771611-C-G

47918936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42771611-C-T

47918964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42771589-G-A

47918970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42771583-T-C

http://identifiers.org/hco/6/GRCh38#47918990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42771567-A-C

47919143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42771426-C-T

47919229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42771359-A-G

47919260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42771340-T-C

47919269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42771331-T-C

http://identifiers.org/hco/6/GRCh38#47920692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42765360-C-A

47920777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42765277-A-G

47920777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42765277-A-T

47920929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42765131-G-A

http://identifiers.org/hco/6/GRCh38#47921198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42764865-C-A

47921321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42764785-T-C

47921322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42764784-C-G

47921453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42764754-C-T

47921469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42764738-C-T

47921475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42764732-G-A

47921487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42764720-A-T

47921490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42764717-A-G

47921567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42764647-A-G

47921585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42764629-G-A

47921585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42764629-G-T

47921614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42764600-G-A

47921681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42764545-C-T

47922250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42763657-G-A

47922269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42763642-G-C

47922283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42763628-G-A

47922423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42763459-T-G

http://identifiers.org/hco/6/GRCh38#47922463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42763419-C-A

47922463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42763419-C-T

47922485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42763397-T-C

47922493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42763387-A-G

47922554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42763315-G-A

47922674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42763207-C-G

47922736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42763144-C-T

47922802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42763083-G-A

47922802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42763083-G-C

47922885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42763000-C-T

47923041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42762824-G-C

47923047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42762818-G-A

47923230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42762678-T-C

47923249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42762663-A-G

http://identifiers.org/hco/6/GRCh38#47923300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42762622-A-C

47924549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42762557-G-A

47924561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42762545-G-A

47924642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42762463-C-G

47924658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42762447-A-T

47925553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42761663-C-G

47925553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42761663-C-T

47925568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42761648-C-T

http://identifiers.org/hco/6/GRCh38#47925716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42761493-C-A

http://identifiers.org/hco/6/GRCh38#47925777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42761455-C-A

47925924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42761296-C-T

47925982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42761232-G-A

47925982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42761232-G-T

http://identifiers.org/hco/6/GRCh38#47926114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42761100-C-A

47926993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760850-G-A

47927020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760822-A-G

47927104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760743-T-C

47927204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760651-C-T

47927209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760646-T-C

47927243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760614-G-A

47927358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760511-C-T

47927373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760496-A-G

47927454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760414-C-G

47927986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760306-T-G

47928027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760264-A-G

47928027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760264-A-T

47928045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760251-C-T

47928056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760240-C-G

47928111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760183-C-T

47928287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760032-G-A

47928287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42760032-G-T

47928363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42759967-A-G

47928394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42759936-A-G

47928445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42759921-T-C

47928516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42759851-T-C

47928665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42759608-G-A

47928757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42759507-G-A

47929027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42759269-T-C

47929112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42759181-C-T

47929245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42759047-G-A

47929245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42759047-G-C

47929335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758954-G-A

http://identifiers.org/hco/6/GRCh38#47929357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42758932-C-A

47929372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758917-T-C

47929381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758908-C-T

47929408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758882-G-A

47929447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758843-G-C

47929447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758843-G-T

47929519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758767-T-C

47929600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758651-G-C

47929653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758598-C-G

47929673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758578-C-T

47929784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758469-C-T

http://identifiers.org/hco/6/GRCh38#47929829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42758417-C-A

http://identifiers.org/hco/6/GRCh38#47929893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42758372-A-C

47929923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758350-C-T

47929929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758344-C-T

47930117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758151-T-A

47930117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758151-T-C

47930118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758150-A-G

http://identifiers.org/hco/6/GRCh38#47930129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42758139-A-C

47930162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42758083-G-A

47930651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42757794-T-C

47931186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42755643-C-T

47931275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42755548-C-T

47931418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42755406-G-A

47931431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42755393-T-C

47931837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42755007-C-T

47932785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42746030-A-G

47932866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42745953-A-G

47933002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42745829-C-T

http://identifiers.org/hco/6/GRCh38#47933057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42745767-C-A

47933448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42745425-G-A

47933648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42745211-T-C

http://identifiers.org/hco/6/GRCh38#47933813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42745061-C-A

47933814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42745060-A-T

47933836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42745048-T-C

47933987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42744933-T-C

47934059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42744870-T-A

47934434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42744822-T-C

47934434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42744822-T-G

47935021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42744235-T-C

http://identifiers.org/hco/6/GRCh38#47935101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42744176-C-A

47935168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42744110-T-C

47935547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42743760-A-G

47935669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42743657-G-C

47935669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42743657-G-T

http://identifiers.org/hco/6/GRCh38#47935769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42743553-C-A

47935948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42743378-G-A

47935973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42743253-G-A

http://identifiers.org/hco/6/GRCh38#47935998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42743222-C-A

47936000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42743191-T-C

47936046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42743109-G-A

http://identifiers.org/hco/6/GRCh38#47936074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42743081-A-C

47936363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42742649-A-G

47936584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42742330-T-G

47936671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42742252-A-G

47936680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42742243-G-T

http://identifiers.org/hco/6/GRCh38#47936877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42742044-A-C

47937026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42741893-A-G

47940292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42741535-T-G

47940670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42741182-A-T

http://identifiers.org/hco/6/GRCh38#47940793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42741060-A-C

47940870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42740983-T-C

47940901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42740953-A-G

47941164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42740699-G-T

http://identifiers.org/hco/6/GRCh38#47941214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42740650-C-A

47941224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42740641-A-G

47941454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42740441-C-G

47941527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42740364-C-T

47941555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42740337-A-T

47941942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42739367-C-T

47941992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42739317-C-T

47942019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42739292-T-C

47942071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42739246-C-T

47942090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42739196-C-T

47942331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42738951-C-T

47942463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42738463-T-C

47942845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42738173-T-C

47949179-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42736111-T-A

47949229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42736063-G-A

47949368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42735918-G-A

47949412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42735881-C-T

http://identifiers.org/hco/6/GRCh38#47949493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42735801-C-A

47949493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42735801-C-G

47949493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42735801-C-T

47949631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42735657-T-C

47951075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42734808-A-T

47951121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42734774-T-C

47951273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42734703-G-A

http://identifiers.org/hco/6/GRCh38#47951286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42734694-A-C

47951410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42734571-G-A

47951417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42734564-T-C

47951419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42734562-T-C

47951646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42733587-G-T

http://identifiers.org/hco/6/GRCh38#47951921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42733340-C-A

47952087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42733202-A-G

47952619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42731986-C-G

47952653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42731960-T-C

http://identifiers.org/hco/6/GRCh38#47953152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42731643-C-A

47953241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42731541-T-C

http://identifiers.org/hco/6/GRCh38#47953263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42731519-A-C

47953355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42731430-T-C

47953730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42731055-G-C

47953793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42730992-T-C

47953884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42730882-T-A

47953943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42730831-A-G

47954612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42730162-G-T

47954671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42730103-T-C

47954680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42730094-T-C

47957911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42729353-T-C

47957982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42729280-C-T

47958006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42729256-A-T

47958076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42729190-T-G

47958124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42729157-G-T

47958199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42729089-A-G

47958233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42729051-T-C

47958468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42728863-C-T

47958492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42728843-A-G

47958530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42728805-G-A

47958586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42728750-T-C

47958690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42728657-G-A

47958728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42728619-A-T

47958783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42728563-A-G

47958903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42728374-T-C

47959488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42727943-G-A

47959537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42727904-G-C

47959644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42727787-A-G

47959797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42727641-T-G

47959798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42727640-C-T

47964377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42726076-G-A

47964528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42725921-T-A

47964594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42725869-C-T

47964714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42725761-G-C

47964951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42725524-G-T

http://identifiers.org/hco/6/GRCh38#47965003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42725485-C-A

47965003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42725485-C-T

47965023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42725468-G-A

47965023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42725468-G-T

47965127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42725407-T-C

47965148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42725386-G-A

47965253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42725272-G-A

47965356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42725160-T-C

47969129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42723382-C-G

47969129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42723382-C-T

47969199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42723335-C-T

47969234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42723304-C-T

47969333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42723202-C-T

47969409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42723134-C-T

http://identifiers.org/hco/6/GRCh38#47969891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42722145-C-A

47969926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42722110-G-A

47970024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42722014-A-G

47970083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42721963-C-G

47970083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42721963-C-T

47970130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42721916-G-C

47970327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42721732-G-A

47970967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42721496-C-G

http://identifiers.org/hco/6/GRCh38#47971088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42721386-C-A

47971088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42721386-C-T

47971178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42721310-G-C

47971213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42721275-A-G

http://identifiers.org/hco/6/GRCh38#47971269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42721219-C-A

47971269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42721219-C-T

47971291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42721206-A-G

47971299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42721198-A-G

http://identifiers.org/hco/6/GRCh38#47971529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42720976-A-C

http://identifiers.org/hco/6/GRCh38#47971580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42720913-A-C

47971876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42720476-G-A

47972000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42720362-A-T

http://identifiers.org/hco/6/GRCh38#47972228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42720151-A-C

47972416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42719997-T-C

47972559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42719859-A-G

47972620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42719804-A-G

47972737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42719642-A-G

47973011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42719390-A-G

http://identifiers.org/hco/6/GRCh38#47973089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42719326-A-C

47973104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42719319-G-A

47973193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42719220-T-C

47973220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42719198-T-C

http://identifiers.org/hco/6/GRCh38#47973357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42719052-C-A

47973442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718972-G-A

47973527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718911-C-G

47973527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718911-C-T

47973556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718882-C-T

47973625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718815-C-T

47973773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718639-A-G

47973782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718607-T-G

http://identifiers.org/hco/6/GRCh38#47973951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42718453-A-C

47973986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718413-G-A

47974120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718308-T-C

47974245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718188-G-T

47974366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718085-A-G

47974370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718081-A-T

47974383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718068-G-A

47974383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42718068-G-C

47974733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42717794-G-T

47974735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42717791-T-C

http://identifiers.org/hco/6/GRCh38#47974966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42717600-A-C

47975048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42717536-A-T

47975629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42716502-T-A

47975629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42716502-T-C

47975638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42716493-G-A

47975706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42716421-G-A

47975717-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42716411-T-G

http://identifiers.org/hco/6/GRCh38#47975990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42716364-C-A

47976048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42716306-G-A

47976096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42716262-T-C

47976284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42716068-A-G

47980208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42715707-G-A

47980232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42715687-A-G

47980263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42715615-C-T

47980307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42715516-T-G

47980369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42715454-C-T

47980440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42715401-G-T

47980568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42715277-A-T

47980676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42715171-A-G

47980785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42715061-C-T

47980842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42714993-A-T

47980958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42714815-C-T

47981144-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42714581-T-G

47981330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42714412-C-T

47981602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42714175-T-C

47982082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42713776-C-T

47985075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42711676-C-T

http://identifiers.org/hco/6/GRCh38#47985149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42711598-A-C

47985428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42711344-A-G

47985453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42711319-G-A

47985773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42711033-G-T

47985780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42711026-G-A

47985868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42710901-G-A

47985868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42710901-G-T

47985896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42710702-A-T

47986012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42710586-T-A

47986312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42710268-A-G

http://identifiers.org/hco/6/GRCh38#47986517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42710096-A-C

47986541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42710057-G-A

47986542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42710054-G-T

47986577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42710017-G-T

47992915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42706525-A-G

47993046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42706397-C-T

47993125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42706317-G-A

47993260-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42706177-T-A

47993260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42706177-T-C

47993486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42705932-A-G

47993519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42705899-T-C

47993777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42704800-G-A

http://identifiers.org/hco/6/GRCh38#47993841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42704735-A-C

47993994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42704580-G-A

47994019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42704556-C-T

47994965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42703592-A-G

47995028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42703522-A-T

47995213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42703413-T-C

47995311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42703304-C-G

47995311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42703304-C-T

47995481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42703139-C-T

47995611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42703022-T-C

47995675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42702966-G-A

http://identifiers.org/hco/6/GRCh38#47995699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42702939-C-A

47995699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42702939-C-T

47995770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42702868-G-A

47996009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42702706-A-G

47996479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42702419-G-A

47996499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42702399-C-G

47996499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42702399-C-T

47996810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42702129-C-T

47996932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42702025-A-G

47997041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42701112-A-G

http://identifiers.org/hco/6/GRCh38#47997143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42701012-C-A

47997197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42700949-T-C

47997214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42700933-G-A

47997214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42700933-G-T

47997230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42700918-T-A

47997346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42700809-C-G

47997412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42700742-C-G

47997412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42700742-C-T

47997429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42700712-A-G

47997471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42700672-T-C

47997549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42700595-G-A

47997549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42700595-G-T

47997604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42700549-G-A

47997692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42700455-A-G

47997728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42699734-C-G

47997739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42699723-A-G

47997802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42699661-G-T

47997882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42699586-A-T

47997965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42699505-C-T

47998040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42699406-T-C

47998156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42699319-G-A

47998235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42699233-G-A

47998288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42699182-G-A

47998482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42698995-A-G

47998543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42698935-T-C

47998544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42698934-G-C

http://identifiers.org/hco/6/GRCh38#47998597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42698881-A-C

47998619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42698642-A-G

47999069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42696565-A-G

48005023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42691798-A-T

48005040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42691781-T-A

48005040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42691781-T-C

48005102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42691699-G-A

48005290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42691524-T-C

48005599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42690782-T-C

48005621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42690764-C-G

48005794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42690585-G-A

48005794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42690585-G-T

48005830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42690551-C-T

48006108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42690368-C-T

48006342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42690172-T-C

48006384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42690121-T-C

48006533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42690006-G-C

48006533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42690006-G-T

48006585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42689944-T-C

http://identifiers.org/hco/6/GRCh38#48006785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42689761-C-A

48006832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42689717-G-A

48006892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42689666-T-G

48007556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42690172-T-C

48007583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42690145-C-T

48007587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42690133-T-C

48007771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42689367-C-T

48007803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42689343-A-G

48007827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42689322-T-C

48008091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42689100-T-C

48008149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42689026-C-G

48008383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42688787-G-C

http://identifiers.org/hco/6/GRCh38#48008495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42688674-C-A

48008495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42688674-C-G

48008495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42688674-C-T

48008518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42688643-A-G

48008526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42688635-A-G

48008547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42688614-A-G

http://identifiers.org/hco/6/GRCh38#48008560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42688603-C-A

48008560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42688603-C-T

48008619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 42688544-A-G

48008675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: missense variant
orthologous variants: 42688488-T-C

48008795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 42688368-G-T

48008798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 42688365-G-T

48008915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 42688248-T-C

48009110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 42688053-C-T

48009318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42687851-T-A

48009324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42687845-A-G

48009356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42687813-C-T

http://identifiers.org/hco/6/GRCh38#48009538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42687629-C-A

48009577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42687225-A-T

http://identifiers.org/hco/6/GRCh38#48009630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42687166-C-A

48009630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42687166-C-T

48009654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42687147-C-T

48009745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42687059-T-C

48009755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42687049-T-C

http://identifiers.org/hco/6/GRCh38#48009778-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42687015-A-C

48009783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42687010-T-G

48010041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686774-C-T

48010106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686703-T-C

48010128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686681-T-C

48010162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686647-T-C

48010163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686646-A-G

48010186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686622-C-T

48010218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686590-T-C

48010231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686576-T-A

48010294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686516-G-A

48010366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686452-C-T

48010379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686437-G-A

48010533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686327-A-T

48013413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686118-G-C

48013413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42686118-G-T

48013498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42685808-A-G

48013597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42685722-T-C

48013624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42685703-A-G

48013631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42685696-A-G

48013678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42685654-C-T

48013869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42685495-T-G

48013912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42685453-T-C

48014107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42685268-G-T

48014110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42685265-A-T

http://identifiers.org/hco/6/GRCh38#48014117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42685258-C-A

48014254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42685123-A-T

48014274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42685103-T-C

48014363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42685018-G-T

48014514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684864-C-T

48014644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684748-T-C

48014681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684707-G-A

48014764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684625-G-C

48014813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684576-G-C

48014908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684512-G-A

48014967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684476-C-G

48014967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684476-C-T

48015046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684416-C-G

48015046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684416-C-T

http://identifiers.org/hco/6/GRCh38#48015083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42684378-C-A

48015083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684378-C-T

http://identifiers.org/hco/6/GRCh38#48015129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42684330-A-C

48015309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684144-T-A

48015380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684073-T-A

48015426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684028-G-A

48015447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42684006-A-G

48015546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42683910-A-T

48015666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42683764-T-G

48015750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42683679-G-A

48016062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42683450-T-C

48016150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42683309-G-C

48016159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42683300-G-A

http://identifiers.org/hco/6/GRCh38#48016238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42683226-A-C

48016296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42683178-G-A

48016298-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42683176-C-G

48016360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42683119-C-G

48016360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42683119-C-T

48016368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42683111-A-G

http://identifiers.org/hco/6/GRCh38#48016582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42682897-C-A

48016648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42682854-G-A

48016675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42682832-G-A

48016675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42682832-G-T

48016817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42682694-A-G

48016915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42682598-T-A

48016970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42682544-T-C

48016981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42682533-T-C

48016993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42682521-G-A

48017132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42682374-A-G

48017132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42682374-A-T

48017402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42682115-G-A

48017769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42681758-G-T

48017843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42681679-G-A

48017858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42681666-T-C

48017888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42681635-G-A

48018049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42681440-T-C

48018376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42680735-T-C

48018463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42680653-G-A

48018463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42680653-G-T

48018663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42680469-G-T

48018818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42679003-T-C

48018858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42678965-G-A

48018958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42678866-T-C

48019869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42677018-T-A

48020001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42676929-T-A

48020085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42676855-G-A

48020116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42676827-A-G

48020158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42676784-T-C

http://identifiers.org/hco/6/GRCh38#48020598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42676429-A-C

48020599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42676428-A-G

48020960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42676026-G-A

48021497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42675655-T-C

48021559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42675633-A-T

48021623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42675571-C-T

48021911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42675326-T-C

48022185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42674512-T-C

48022352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42674339-C-T

48022441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42674250-A-G

48022572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42674120-T-C

48022686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42674011-G-A

http://identifiers.org/hco/6/GRCh38#48023289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42673486-C-A

http://identifiers.org/hco/6/GRCh38#48023361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42673418-A-C

48023361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42673418-A-G

48023388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42673391-A-G

48023420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42673359-G-A

48023474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42673309-A-G

48023508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42673277-A-G

48023510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42673275-C-G

48023510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42673275-C-T

48023523-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42673262-T-A

48023523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42673262-T-G

48023590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42673195-C-T

48023609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42673176-G-A

48023881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42672735-C-T

48024094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42672527-T-G

48024129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42672495-A-G

48024433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42672183-A-G

http://identifiers.org/hco/6/GRCh38#48024570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42672049-C-A

48025115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42670160-T-C

48025135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42670140-C-T

48025146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42670132-C-T

48025275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42670012-G-T

48025432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42669862-A-G

48025508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42669791-G-A

48025541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42669759-G-T

http://identifiers.org/hco/6/GRCh38#48025720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42669599-C-A

48025720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42669599-C-G

48025821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42669502-G-C

48029104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42668873-T-C

48029162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42668815-A-G

48029210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42668780-T-C

48029391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42668666-A-G

48029420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42668636-G-C

http://identifiers.org/hco/6/GRCh38#48029471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42668588-C-A

48029570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42668426-T-C

48029673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42668340-G-A

48030343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42667839-C-G

48030345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42667837-T-G

48030530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42667661-T-A

48030685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42667517-A-G

http://identifiers.org/hco/6/GRCh38#48031072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42666926-C-A

48031072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42666926-C-T

48031136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42666865-T-A

48031176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42666833-C-G

48031182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42666827-C-G

48031220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42666806-G-C

48031320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42666709-A-G

48031320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42666709-A-T

48031494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42666554-G-A

http://identifiers.org/hco/6/GRCh38#48031601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42666273-C-A

48031601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42666273-C-T

48031605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42666269-G-A

48031605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42666269-G-C

http://identifiers.org/hco/6/GRCh38#48031613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42666262-C-A

http://identifiers.org/hco/6/GRCh38#48031660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42666217-A-C

48031661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42666216-G-A

48031661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42666216-G-T

48032073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42665803-G-A

48032120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42665760-G-A

48032179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42665701-A-G

48032287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42665596-G-A

48032437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42665464-C-T

48032473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42665430-G-A

48032532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42665370-A-G

48032541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42665361-A-T

48032822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42665075-G-A

48033093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42664819-A-G

48033253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42664658-G-T

48033270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42664641-T-A

48033366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42664548-T-C

48033773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42664233-C-T

48033790-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42664223-C-G

http://identifiers.org/hco/6/GRCh38#48033799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42664213-C-A

48033905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42664136-T-G

48033980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42664071-C-T

48034024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42664059-A-G

48034282-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42663822-T-A

48034568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42663022-T-A

48034581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42663009-T-C

48034600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42662989-G-T

48034664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42662866-C-T

48034847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42662686-G-A

48035055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42662481-A-T

48035532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42661127-G-C

48035545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42661114-T-C

48035583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42661072-A-T

48035599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42661056-C-G

48035599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42661056-C-T

48035640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42660989-A-G

48035650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42660981-G-C

http://identifiers.org/hco/6/GRCh38#48035654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42660977-C-A

48035702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42660929-C-G

48035903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42660752-T-G

48035945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42660712-T-C

48035969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42660686-A-G

48035979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42660674-C-T

48036026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42660629-T-A

48036189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42660467-A-G

48036189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42660467-A-T

http://identifiers.org/hco/6/GRCh38#48036195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42660461-A-C

48036209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42660447-G-A

48036209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42660447-G-C

48037502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42659867-T-C

48037516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42659853-T-C

48037516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42659853-T-G

48037536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42659832-C-T

48037596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42659775-T-C

48037614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42659756-G-A

48037710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42659667-T-C

http://identifiers.org/hco/6/GRCh38#48037805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42659575-A-C

48037823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42659561-G-C

48038660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658713-T-C

http://identifiers.org/hco/6/GRCh38#48038661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42658712-C-A

48038661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658712-C-G

48038661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658712-C-T

http://identifiers.org/hco/6/GRCh38#48038663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42658710-C-A

48038682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658691-G-A

48038682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658691-G-T

48038731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658643-A-G

48038808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658564-A-G

http://identifiers.org/hco/6/GRCh38#48038892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42658481-A-C

http://identifiers.org/hco/6/GRCh38#48038893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42658480-A-C

48038893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658480-A-T

48038980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658363-A-G

48039018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658255-C-G

48039018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658255-C-T

48039051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658195-G-C

48039172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658069-T-C

48039195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42658046-T-C

48041093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42655977-A-G

48041206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42655851-T-A

48041228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42655829-A-G

48042237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42654796-T-C

48042396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42654615-T-C

48042562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42654443-A-G

48042572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42654434-C-T

http://identifiers.org/hco/6/GRCh38#48042584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42654422-C-A

48042584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42654422-C-T

http://identifiers.org/hco/6/GRCh38#48042726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42654272-C-A

48042930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42654062-G-A

48042930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42654062-G-C

http://identifiers.org/hco/6/GRCh38#48043006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42654000-C-A

48043006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42654000-C-T

48043035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42653968-G-C

48043110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42653458-A-G

48043626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42652931-G-A

48043754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42652810-T-C

48043945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42652612-G-A

48044149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42652441-T-C

48044269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42652329-G-A

48044461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42651871-G-A

48044499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42651830-T-C

48044563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42651720-G-A

48044567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42651716-T-C

48044639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42651647-T-A

http://identifiers.org/hco/6/GRCh38#48045051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42651366-C-A

48045188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42651236-G-A

http://identifiers.org/hco/6/GRCh38#48045267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42651157-A-C

48045602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42650808-C-T

48045879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42650452-G-C

48045949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42650392-A-G

48045949-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42650392-A-T

48045950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42650391-T-C

48046357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42649653-A-G

48046384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42649523-G-C

48046781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42649145-C-T

48046796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42649131-T-C

48046994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42648983-G-A

48047193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42648766-T-C

48047336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42648596-G-C

48047443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42648495-T-C

48047470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42648469-T-C

48047616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42648321-A-G

48047654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42648286-G-A

48047654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42648286-G-C

48047847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42648129-C-T

48047968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42648008-A-G

48047971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42648005-T-C

http://identifiers.org/hco/6/GRCh38#48048038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42647924-A-C

48048038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42647924-A-G

http://identifiers.org/hco/6/GRCh38#48048039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42647923-C-A

48048039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42647923-C-G

48048120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42647840-G-T

48048499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42647453-T-A

48048499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42647453-T-C

48048576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42647380-C-T

48048592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42647364-G-A

48048592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42647364-G-T

48048640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42647316-G-A

48048846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42647115-T-C

48048857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42647104-G-C

48049174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42646816-T-C

48049380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42646639-T-C

48049689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42646335-C-G

http://identifiers.org/hco/6/GRCh38#48050194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42645873-C-A

http://identifiers.org/hco/6/GRCh38#48050301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42645766-C-A

48050463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42645611-A-G

http://identifiers.org/hco/6/GRCh38#48050672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42645426-C-A

48050672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42645426-C-T

48050684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42645413-A-G

48050687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42645410-A-G

48050728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42645369-T-G

48050729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42645368-G-A

48050797-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42645299-G-C

48051159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42644947-A-G

48051194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42644911-C-T

48051577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: -T-C

http://identifiers.org/hco/6/GRCh38#48051603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42644530-C-A

48051603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42644530-C-T

48051627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42644509-T-A

48051693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42644444-T-C

48052122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42644017-G-A

48052123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42644016-G-A

48052172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42643955-T-C

48052194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42643926-A-G

48052445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42643594-C-G

48052579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42643384-T-C

48052685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42643243-T-C

48052909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42643067-A-G

http://identifiers.org/hco/6/GRCh38#48052971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42643005-A-C

48053108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42642864-G-T

48053174-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42642809-G-C

48053187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42642796-T-A

48053216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42642762-A-G

48053318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42642360-A-T

48053494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42642207-G-A

48053549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42642151-T-C

48053613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42642088-G-A

48053655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42642052-G-T

48053810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42641898-C-T

48053855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42641853-A-G

48053890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42641824-T-A

48053903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42641811-G-A

48054391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42641134-C-T

48054767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42640838-A-G

http://identifiers.org/hco/6/GRCh38#48054963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42640483-C-A

48055023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42640424-T-C

48055432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42639962-G-A

48055810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42639570-G-T

48055886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42639464-T-C

48056053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42639321-A-G

48056103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42639263-A-G

48056113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42639253-T-A

48056168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42639188-G-A

48056527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42638859-T-C

48056529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42638857-G-A

48056721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42638673-G-T

48056733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42638669-C-T

48056757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42638651-C-T

48057009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42638368-C-T

48057378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42637950-G-T

48057809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42637564-G-A

http://identifiers.org/hco/6/GRCh38#48057921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42637462-A-C

48057974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42637409-G-A

48058043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42637338-T-G

48058058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42637323-G-A

48058333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42637092-A-G

48058383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42637070-T-A

48058723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42636736-A-G

48058931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42636542-T-A

48059196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42636309-A-T

48059198-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42636307-T-G

48059306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42636200-A-G

http://identifiers.org/hco/6/GRCh38#48059664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42636147-A-C

48059906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42635910-C-G

48059944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42635875-C-T

48060096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42635751-G-A

48060249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42635592-G-A

48060376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42635486-A-T

48060398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42635463-T-C

48060861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42634978-G-A

48060861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42634978-G-C

48061102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42634767-C-T

48061936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42634348-G-A

48062055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42634222-A-T

48062191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42634109-T-A

48062592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42633455-A-G

48062596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42633451-G-T

48062803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42633300-T-C

http://identifiers.org/hco/6/GRCh38#48062804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42633299-C-A

48063091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42633030-C-T

48063299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42632804-C-G

48063735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42632338-G-A

48063831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42632197-T-G

48064123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631928-T-C

48064258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631826-A-G

48064355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631738-A-G

48064416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631677-C-T

48064459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631634-G-T

48064532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631556-G-A

48064532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631556-G-C

48064547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631526-T-A

48064557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631518-G-A

48064566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631509-T-C

48064652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631452-G-A

48064834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631280-A-G

48064848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631266-G-A

48064892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631222-G-T

48064950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631164-T-C

48065050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631061-A-G

http://identifiers.org/hco/6/GRCh38#48065110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42631004-C-A

48065110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42631004-C-T

48065927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42630214-T-G

48066091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42630045-G-A

48066102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42630034-T-C

48066232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42629960-T-C

48066252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42629940-A-G

48066466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42629735-A-G

48066563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42629645-T-C

48066672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42629537-A-G

48066709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42629497-T-G

48066817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42629405-A-G

48067015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42629216-T-A

48067086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42629138-T-C

http://identifiers.org/hco/6/GRCh38#48067159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42629065-A-C

48067218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42629006-G-A

48067600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42628597-A-T

48067831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42628373-T-A

48067840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42628364-G-A

48067840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42628364-G-T

48067922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42628273-T-G

48067925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42628270-T-C

http://identifiers.org/hco/6/GRCh38#48068315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42627870-A-C

48068315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, missense_variant
orthologous variants: 42627870-A-G

48068495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, missense_variant
orthologous variants: 42627690-A-G

48068495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, missense_variant
orthologous variants: 42627690-A-T

48068589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 42627596-G-A

48068589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 42627596-G-C

48068589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 42627596-G-T

48068721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42627449-T-A

48068721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42627449-T-C

48068722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42627448-C-G

http://identifiers.org/hco/6/GRCh38#48068726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42627444-A-C

48068726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42627444-A-G

http://identifiers.org/hco/6/GRCh38#48068743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42627427-A-C

48068743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42627427-A-T

48068751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42627417-C-T

48068885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42627282-G-T

http://identifiers.org/hco/6/GRCh38#48068903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#42627253-C-A

48068903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron variant
orthologous variants: 42627253-C-T

48069310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42626859-G-A

48069447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42626731-A-G

48069654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42626527-A-G

48069757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42626424-T-A

48069780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42626410-C-G

http://identifiers.org/hco/6/GRCh38#48069798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#42626374-C-A

48069798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42626374-C-T

48069838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 42626313-A-G

48070283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42625915-G-T

48070410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42625780-T-C

48070413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42625777-A-G

48070642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42625557-T-C

48071177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42624807-A-G

48071225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42624759-T-C

48071734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42624282-T-G

http://identifiers.org/hco/6/GRCh38#48071755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#42624261-C-A

48071850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42624162-G-A

48072129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42623913-T-C

48072402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42623524-C-T

48072404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42623522-G-A

48072555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42623327-T-C

48072714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42623121-A-G

48072787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42623056-A-G

48072793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42623050-T-C

48072933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42622904-A-T

48072937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42622900-A-G

48072955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42622880-T-C

48073156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42622692-G-A

48073192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42622656-G-T

http://identifiers.org/hco/6/GRCh38#48073386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#42622492-A-C

48073389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42622489-C-T

48073507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42622378-T-A

48073715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42622220-A-G

48074047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42621922-G-A

48074526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42621291-C-T

48074572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42621245-G-A

48074718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42621112-A-G

48074811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42621017-T-G

48075249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42620643-A-G

48075249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42620643-A-T

48075272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42620621-A-G

48075272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42620621-A-T

48075483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42619912-C-T

http://identifiers.org/hco/6/GRCh38#48075488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#42619907-C-A

48075519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42619876-G-T

48078109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42619830-G-C

48078155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42619784-G-T

48078324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42619626-A-G

48078707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42619268-C-G

48078707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42619268-C-T

48079228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42619058-G-A

48079247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42619039-G-T

48079467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42618830-A-G

http://identifiers.org/hco/6/GRCh38#48079605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#42618699-C-A

48079605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42618699-C-G

48079627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42618693-T-C

48079652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42618668-A-G

48079709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42618613-T-C

48079769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42618555-T-G

48079852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42618471-C-T

48079970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42618339-A-T

48080008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42617967-G-A

48080008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42617967-G-T

48080037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42617947-T-C

48080044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42617940-G-A

48080416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42617532-T-A

48080487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42617462-T-C

48080487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42617462-T-G

48087505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42615510-G-A

http://identifiers.org/hco/6/GRCh38#48087833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#42615196-C-A

48087855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42615175-T-C

48087969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42615071-G-A

48088247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42614876-A-G

48088351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42614774-T-C

48088533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42614598-G-A

48089262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42614198-C-G

48089478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42613959-A-T

48090076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42611739-T-C

48090390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42611321-G-A

48090537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42611065-G-A

48090537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42611065-G-T

48091341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42610329-G-T

48091626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42610011-T-A

48091626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42610011-T-C

48091678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42609965-G-A

48091890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42609735-T-A

48091938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42609688-C-T

http://identifiers.org/hco/6/GRCh38#48092496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#42609481-C-A

48092624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42609355-T-G

48092687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42609291-G-A

48093320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42608757-A-G

48094109-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42607324-T-A

48094333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42607144-T-C

48094485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42606993-A-G

http://identifiers.org/hco/6/GRCh38#48094699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#42606778-A-C

48094902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42606557-A-G

http://identifiers.org/hco/6/GRCh38#48095718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#42605969-C-A

48095793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42605894-T-A

48095793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42605894-T-C

48095993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42605739-T-C

48096238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42605489-G-C

http://identifiers.org/hco/6/GRCh38#48097753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#42598693-A-C

48098733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42597711-T-C

48098733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42597711-T-G

http://identifiers.org/hco/6/GRCh38#48098923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#42597606-C-A

48099034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42597484-T-C

48099329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42597184-G-A

48099704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42596787-G-A

http://identifiers.org/hco/6/GRCh38#48099705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#42596786-C-A

48099705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42596786-C-T

48099706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42596785-A-G

48099875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42596622-C-T

48099973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42596525-G-A

48111002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: intron_variant, undefined
orthologous variants: 42589039-C-T

48111052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 42588988-C-T

48111176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42588866-A-G

48111178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21345
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42588864-C-T