181875102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544332-G-C

181875354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544076-T-C

181875394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544038-A-G

181875434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544000-A-G

181875434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49544000-A-T

http://identifiers.org/hco/4/GRCh38#181875455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49543995-C-A

181875455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543995-C-G

181875455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543995-C-T

181875459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543991-C-T

181875638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543824-T-C

181875695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543776-T-C

http://identifiers.org/hco/4/GRCh38#181875733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49543739-A-C

http://identifiers.org/hco/4/GRCh38#181875800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49543677-C-A

181876103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543419-T-C

181876201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543320-T-C

181876248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543273-T-C

181876353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543168-T-C

181876445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543078-A-G

181876527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49543001-A-T

181876982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49542549-A-G

181877187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49542320-G-A

181877188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49542319-G-A

181877192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49542315-A-G

181877220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49542293-G-T

181877325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49542209-A-G

181877550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541972-C-G

181877550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541972-C-T

181877616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541901-G-C

181877649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541874-C-T

181877782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541740-G-A

181877879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541570-T-C

181877879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541570-T-G

181878006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541455-G-A

181878024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541437-G-A

181878353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541082-G-T

181878373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541062-G-A

181878399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49541039-T-C

181878768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49540757-C-T

181878795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49540733-C-T

181878801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49540724-A-G

181878821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49540704-A-G

181879098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49540443-T-C

181879114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49540370-G-A

181879137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49540349-G-A

181879144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49540342-T-C

181879411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49540090-G-T

181879493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539998-G-C

http://identifiers.org/hco/4/GRCh38#181879494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49539997-A-C

181879494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539997-A-G

181880259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539171-A-G

181880283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539147-T-C

181880294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49539136-G-A

181880917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49538222-A-T

http://identifiers.org/hco/4/GRCh38#181880921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49538216-C-A

http://identifiers.org/hco/4/GRCh38#181881183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49537993-C-A

181881183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537993-C-T

http://identifiers.org/hco/4/GRCh38#181881216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49537960-C-A

181881216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537960-C-T

181881367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537813-G-A

181881508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537713-A-T

181881510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537711-T-A

181881571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537670-G-T

181881586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537655-C-G

http://identifiers.org/hco/4/GRCh38#181881707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49537530-A-C

181881707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537530-A-G

181881811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537432-T-C

181881856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537388-G-A

181881856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537388-G-T

http://identifiers.org/hco/4/GRCh38#181882067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49537163-A-C

181882067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537163-A-G

181882131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537098-G-T

181882162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537066-A-G

181882197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49537002-G-A

181882398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536804-A-G

http://identifiers.org/hco/4/GRCh38#181883109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49536234-C-A

181883109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536234-C-T

181883173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536153-T-C

181883259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49536071-G-T

181883359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535917-A-G

181883388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535888-T-C

http://identifiers.org/hco/4/GRCh38#181883768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49535797-C-A

181883848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535726-T-C

181883910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535665-T-A

181883960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535616-T-C

http://identifiers.org/hco/4/GRCh38#181883979-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49535597-A-C

181883979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535597-A-T

181883987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535589-C-G

181883994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535582-G-T

181884117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535462-T-G

181884185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535397-C-G

181884254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535351-C-T

http://identifiers.org/hco/4/GRCh38#181884589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49535041-C-A

181884590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49535040-A-T

181887194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49533008-C-T

181887871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49525087-C-T

181887877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49525081-G-A

181889516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524229-G-T

181889520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524225-G-T

181889537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524208-T-C

181889567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49524181-G-A

181889749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49523998-G-A

181890186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49523566-C-G

181890288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49523463-T-A

181890288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49523463-T-C

http://identifiers.org/hco/4/GRCh38#181890536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49523221-C-A

181891216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49522562-A-G

http://identifiers.org/hco/4/GRCh38#181892267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49521063-C-A

181892548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49520353-A-T

http://identifiers.org/hco/4/GRCh38#181892637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49519066-C-A

181892637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49519066-C-G

http://identifiers.org/hco/4/GRCh38#181892842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49518843-A-C

http://identifiers.org/hco/4/GRCh38#181892948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49518737-C-A

181893258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518434-C-T

181893412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518247-T-C

http://identifiers.org/hco/4/GRCh38#181893482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49518169-C-A

181893482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518169-C-T

181893486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518165-T-A

181893486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518165-T-C

181893486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518165-T-G

181893628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518058-T-C

181893654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518032-A-G

181893673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49518013-A-G

181893784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517906-T-C

181893978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517394-A-G

http://identifiers.org/hco/4/GRCh38#181893995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49517378-C-A

181893995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517378-C-T

http://identifiers.org/hco/4/GRCh38#181894094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49517287-A-C

181894173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49517232-A-G

181894799-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516628-A-T

http://identifiers.org/hco/4/GRCh38#181894892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49516536-C-A

181895061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516364-A-G

181895130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516297-A-T

181895144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516283-A-G

181895171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516261-G-A

181895412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516031-T-A

181895432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49516014-C-G

http://identifiers.org/hco/4/GRCh38#181895483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49515973-C-A

181895547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515936-T-A

181895742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515891-C-T

181895884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515803-C-T

181895910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515766-G-T

181896467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515181-C-G

181896513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49515133-G-C

181896673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514983-T-C

181896792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514847-T-C

181896793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514846-G-A

181896827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514812-C-G

http://identifiers.org/hco/4/GRCh38#181896975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49514651-C-A

181897010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514616-T-G

181900102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49514273-G-C

181900138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49513992-A-G

181900138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49513992-A-T

181900272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49513828-T-C

181900272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49513828-T-G

181900301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49513791-A-G

http://identifiers.org/hco/4/GRCh38#181900619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49513467-C-A

181900623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49513463-A-G

181900752-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49513337-T-G

181900783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49513306-T-C

181900905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49513162-G-T

181901081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49512444-G-A

181901081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49512444-G-T

http://identifiers.org/hco/4/GRCh38#181901546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49511871-A-C

181901546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49511871-A-G

181901833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49511583-A-G

181902173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49511250-T-A

181902856-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49510955-C-G

181902900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49510908-A-T

181903254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49510409-A-G

181903264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49510399-T-C

181903501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49510151-G-T

181903586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49510069-T-A

181903586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49510069-T-C

181903599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49510056-T-G

181903955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509721-A-T

181904116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509583-A-G

181904160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509520-C-T

181907539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509082-T-C

181907549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509072-C-T

181907590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49509032-G-A

181908169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49508324-C-G

181908229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49508265-G-A

http://identifiers.org/hco/4/GRCh38#181908239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49508255-A-C

181908362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49508145-G-A

181908363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49508144-A-T

181908491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49508018-G-A

181908491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49508018-G-T

181908703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507803-T-C

181910718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49507360-C-T

http://identifiers.org/hco/4/GRCh38#181911266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49506855-C-A

181911357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506764-C-G

181911687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49506433-A-G

181914981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505770-G-A

181915012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505739-C-T

181915113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505635-G-A

181915113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505635-G-T

181915314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505441-C-T

181915317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505438-T-G

181915438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505323-T-G

http://identifiers.org/hco/4/GRCh38#181915596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49505170-A-C

181915615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505151-T-A

181915701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49505015-G-A

181915901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49504778-A-G

181916124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49504553-C-T

181916423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49504300-G-T

181916449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49504274-T-C

181916497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49504229-A-T

181918159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49501651-A-G

181918285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49501526-G-A

181918285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49501526-G-C

181918327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49501484-T-A

181918344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49501467-C-T

181918528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49501289-G-A

181918759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500661-A-G

181918793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500631-G-T

181918872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49500550-C-T

http://identifiers.org/hco/4/GRCh38#181923796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49500117-A-C

181924060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49499800-C-G

181924594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49499076-A-G

181924638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49499035-T-G

181924759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49498870-G-C

181924760-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49498869-A-T

181924820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49498811-T-C

181924868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49498766-G-A

181925716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49497903-T-A

181925800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49497821-A-G

181925833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49497789-A-G

181925899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49497719-A-G

181925994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49497632-C-T

181926025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49497601-C-T

181926107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49497526-A-G

181926121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49497512-A-G

181926197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49497441-A-T

181926318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49497304-G-A

181926324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49497298-A-G

181926337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49497286-A-G

181926436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49497195-A-G

181933323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49496922-T-C

181933726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49496506-T-C

181933769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49496460-T-G

181933929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49496324-T-A

181933959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49496295-T-C

181933964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49496290-T-G

181934080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49496061-G-A

181934128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49496023-A-G

181934137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49496014-T-C

181934872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49495274-A-G

181935463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49494176-A-G

181935513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49494126-G-A

181935513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49494126-G-T

181935579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49494059-C-T

181935858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49493798-G-C

181935858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49493798-G-T

181935863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49493793-A-T

181936802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49492970-G-T

181936883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49492913-G-A

181936884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49492912-G-C

181937844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49490696-A-G

181937870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49490671-C-G

181937870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49490671-C-T

181938356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49489746-A-G

181938478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49489637-C-T

181938553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49489554-T-C

http://identifiers.org/hco/4/GRCh38#181939053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49489038-A-C

181939053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49489038-A-G

181939688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49488255-G-A

181939702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49488241-T-G

181939925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49488041-G-C

181940031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49487951-G-A

http://identifiers.org/hco/4/GRCh38#181940073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49487910-C-A

181940177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49487692-T-C

181940278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49487587-A-T

181940371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49487502-T-C

181940385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49487488-T-C

181940385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49487488-T-G

http://identifiers.org/hco/4/GRCh38#181940422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49487451-C-A

181940422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49487451-C-T

181940759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49486882-G-T

181940773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49486861-A-G

181940799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49486834-G-T

181940829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49486804-A-G

181940971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49486677-T-C

http://identifiers.org/hco/4/GRCh38#181941206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49485613-A-C

http://identifiers.org/hco/4/GRCh38#181941371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49485477-A-C

181941737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49485081-A-G

181941822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49484999-T-C

181942291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49484376-T-A

http://identifiers.org/hco/4/GRCh38#181942309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49484358-C-A

181942309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49484358-C-T

181942373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49484288-G-A

181942385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49484276-G-A

181942451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49484232-G-A

http://identifiers.org/hco/4/GRCh38#181942552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49484137-A-C

181942803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49483882-C-T

181943039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49483657-C-G

181943158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49483533-G-A

181943207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49483483-A-T

181943321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49483408-T-C

181943452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49483289-T-C

181944051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49482556-T-C

181944376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49482218-C-T

181944382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49482212-T-C

181944658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49481964-C-T

181946163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49481198-C-T

181946296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49481109-A-G

http://identifiers.org/hco/4/GRCh38#181946413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49480995-C-A

181946498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49480824-T-G

181946512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49480808-A-G

181946549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49480771-A-G

181946722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49480608-T-C

181947106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49480253-C-T

181947144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49480215-C-G

181947370-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49480019-A-T

http://identifiers.org/hco/4/GRCh38#181947669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49479596-A-C

181947689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479577-G-A

http://identifiers.org/hco/4/GRCh38#181947735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49479533-A-C

181947740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479531-C-T

181948067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49479188-A-G

181948267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49478988-G-T

181948733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49478622-T-C

181948752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49478603-A-T

181948922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49478434-G-C

181948930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49478426-A-G

181949029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49478319-G-A

181949067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49478215-A-G

181949079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49478203-C-T

181949109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49478170-T-C

181949294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49477989-A-G

181949433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49477849-T-G

181949534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49477761-G-C

181950132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49477184-C-T

181950294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49477037-C-G

181950328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49476999-G-A

http://identifiers.org/hco/4/GRCh38#181950595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49476737-A-C

181950657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49476673-G-A

181950977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49476468-A-G

181951270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49476337-G-T

181951390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49476207-C-G

181951390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49476207-C-T

181951391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49476206-T-C

181951397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49476200-A-G

181951910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49475676-G-A

181952201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49475324-T-C

181952201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49475324-T-G

http://identifiers.org/hco/4/GRCh38#181952563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49474968-A-C

181952752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49474786-G-A

181952787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49474748-A-G

181952854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49474711-C-T

181952917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49474668-G-A

181952925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49474662-T-C

181953028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49474584-C-T

181953045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49474551-G-A

181953194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49474387-C-T

181953385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49474227-A-G

http://identifiers.org/hco/4/GRCh38#181954877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49472358-C-A

http://identifiers.org/hco/4/GRCh38#181954926-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49472323-C-A

181955093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49472170-A-T

181955191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49472011-A-G

181955251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49471875-C-T

181955288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49471820-G-T

181955289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49471819-T-C

181955385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49471661-C-T

181955404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49471642-G-C

181955412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49471634-A-G

http://identifiers.org/hco/4/GRCh38#181955504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49471544-C-A

181955620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49471427-A-G

181955667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49471381-G-T

181955672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49471376-T-C

181955710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49471341-G-A

181955730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49471326-G-A

181955802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49471266-T-C

181956034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49471026-G-A

181956080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49470980-G-A

181956383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49470524-C-T

181956390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49470517-G-A

181956496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49469324-A-G

181956710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49469101-T-C

181956911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49468892-T-C

181956989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49468812-A-G

181956995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49468801-C-T

181957180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49468491-G-T

181957247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49468424-A-G

181957423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49468246-G-A

181957624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49468054-A-G

181957626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49468052-T-A

181957679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49467999-T-C

181957766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49467912-T-C

181958435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49467104-T-A

181958483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49467055-G-A

181958521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49467017-T-C

181958549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49466989-G-A

181958658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49466882-C-G

181960090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49464807-C-G

181960093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49464804-C-T

181960465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49464427-C-T

181960594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49464298-A-G

181960594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49464298-A-T

181960713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49464178-C-T

http://identifiers.org/hco/4/GRCh38#181960718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49464173-A-C

181960718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49464173-A-G

http://identifiers.org/hco/4/GRCh38#181960792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49464098-A-C

181960939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49463952-G-C

181960939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49463952-G-T

181960965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49463926-A-G

181961236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49463653-C-T

181961724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462865-G-A

181961724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462865-G-T

181961730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462859-A-T

181961748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462841-G-A

181961830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462760-G-C

181962384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49462111-G-A

181962584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461905-C-T

http://identifiers.org/hco/4/GRCh38#181962642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49461846-C-A

181962642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461846-C-T

181962872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461623-A-G

181962950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461554-T-G

181963127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49461375-C-T

181963960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49460541-T-C

181964112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49460389-T-G

http://identifiers.org/hco/4/GRCh38#181964215-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49460285-A-C

181964341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49460206-C-T

181964518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49460025-C-T

181964606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49459942-G-A

http://identifiers.org/hco/4/GRCh38#181964744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49459809-C-A

181964843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49459698-A-G

181964869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49459676-T-C

181964908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49459637-A-G

http://identifiers.org/hco/4/GRCh38#181965030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49459516-A-C

181965030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49459516-A-G

181965030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49459516-A-T

181965555-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49458381-T-A

181965555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49458381-T-C

181965654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49458280-A-G

http://identifiers.org/hco/4/GRCh38#181965841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49458124-C-A

181965841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49458124-C-T

181966952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49457019-C-T

181967110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49456855-G-A

181967296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49456697-A-T

181967567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49456436-C-T

181967624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49456388-C-T

http://identifiers.org/hco/4/GRCh38#181967992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49456092-C-A

181968027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49456043-T-C

181968313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49454804-G-A

181968335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49454787-G-A

181968361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49454761-C-T

181968371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49454751-G-A

181968493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49454602-C-G

181968695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49454408-G-A

181968718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49454390-C-T

181968827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49454307-C-T

181969036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49454241-A-G

181969176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49454139-C-G

181969634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49452873-T-C

181969920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49452603-G-T

http://identifiers.org/hco/4/GRCh38#181970204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49452312-A-C

181970424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49452092-C-T

http://identifiers.org/hco/4/GRCh38#181970653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49451862-C-A

181970806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49451717-A-G

181970806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49451717-A-T

181976794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49448029-G-A

181976811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49448011-G-A

181976825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49448000-C-G

181976974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49447702-A-G

181977096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49447548-C-G

181977151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49447494-C-G

181977151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49447494-C-T

181977159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49447486-C-G

http://identifiers.org/hco/4/GRCh38#181977303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49447387-A-C

181977334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49447361-G-A

181977340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49447355-T-G

181977423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49447276-T-C

181977701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49447038-G-A

181977726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49447015-G-A

181977941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49446827-G-A

181977953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49446815-A-G

181978034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49446729-A-G

181978193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49446577-G-C

181978825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49446294-G-T

http://identifiers.org/hco/4/GRCh38#181978970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49446225-C-A

181978970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49446225-C-T

181979076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49446132-T-C

181979178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49446076-G-C

181979523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49445741-G-A

181979523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49445741-G-C

181979571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49445702-T-C

181979633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49445631-G-A

181979639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49445625-T-C

181979663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49445601-T-A

181979663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49445601-T-C

181979668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49445596-T-A

181979679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49445581-C-T

181979686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49445574-C-G

181979757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49445511-G-A

181979780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49445481-C-G

181979780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49445481-C-T

181980160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49444935-A-G

181980238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49444844-G-A

181980238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49444844-G-T

http://identifiers.org/hco/4/GRCh38#181980259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49444823-C-A

181980271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49444812-A-G

181980350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49444751-T-C

181980358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49444743-A-G

181980370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49444731-G-C

181980471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49444628-A-G

http://identifiers.org/hco/4/GRCh38#181980527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49444574-C-A

181980527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49444574-C-T

181980555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49444546-G-A

181980709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49437202-A-G

181980709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49437202-A-T

181980784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49437111-T-A

181980810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49437085-T-C

http://identifiers.org/hco/4/GRCh38#181980922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49436980-A-C

181981015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49436919-G-A

181981015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49436919-G-C

181981382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49436617-G-A

181981382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49436617-G-C

181981436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49436107-G-A

181981634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49435911-G-C

181981789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49435736-G-A

181981810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49435715-T-G

181981904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49435640-G-A

181982072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49435460-C-G

http://identifiers.org/hco/4/GRCh38#181982196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49435336-A-C

181982507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49435008-C-T

http://identifiers.org/hco/4/GRCh38#181982699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49434818-A-C

181982699-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49434818-A-T

181983049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49434468-C-G

181983151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49434367-T-C

181983254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49434266-C-T

181983258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49434262-C-G

181983427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49434090-A-T

181983502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49434012-A-G

http://identifiers.org/hco/4/GRCh38#181983878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49433498-A-C

181983878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49433498-A-G

181984019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49433353-C-T

181984124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49433222-G-A

181984141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49433205-C-T

181984182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49433165-G-A

181984677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49432623-T-C

181984788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49432511-T-A

181984885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49432436-A-G

http://identifiers.org/hco/4/GRCh38#181984941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49432376-A-C

181985044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49432274-A-G

181985124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49432207-T-C

181985282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49432046-G-A

181985480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49431849-G-C

181985725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49431583-G-A

181985725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49431583-G-T

181985811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49431500-G-A

181985835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49431476-G-A

181986940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49428820-G-T

181987001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49428767-A-G

181987292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49428445-G-C

181987465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49428274-T-G

181987562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49428183-A-G

181987731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49427962-T-A

181987735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49427958-G-A

181987750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49427940-C-T

181987764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49427852-A-T

181987836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49427768-A-G

181987872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49427733-G-C

181987872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49427733-G-T

http://identifiers.org/hco/4/GRCh38#181988392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49427216-C-A

181988756-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49426955-A-T

181989015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49426772-A-G

181989092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49426696-C-T

181989112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49426687-T-A

181989112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49426687-T-C

181989206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49426593-A-T

181989537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49425950-A-G

181989962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49425548-G-A

181990141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49425367-T-C

181990456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49425053-T-A

181990577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49424935-G-A

181990577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49424935-G-T

181990847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49424653-G-A

181991219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49424236-C-T

181991819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49423654-A-T

http://identifiers.org/hco/4/GRCh38#181992354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49423116-A-C

181992375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49423095-G-A

181992497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49422972-T-C

181992550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49422916-T-C

181992667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49422785-A-G

181992694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49422756-G-T

181993617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49421809-G-T

181993794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49421632-A-G

181994034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49421373-A-T

http://identifiers.org/hco/4/GRCh38#181994058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49421344-C-A

181994058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49421344-C-G

181994197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49421193-T-A

181994350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49421051-G-T

181994489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49420911-C-T

181994869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49420567-A-G

181995637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49420109-A-G

181996637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49417888-C-T

181996804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49417719-G-A

181997074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49417473-G-T

181997184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49417365-T-C

http://identifiers.org/hco/4/GRCh38#181997241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49417307-A-C

181997245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49417303-G-C

181997340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49417052-G-C

181997382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49417013-G-C

181997461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49416933-G-T

181997524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49416874-T-C

181997540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49416856-C-T

181997789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49416611-G-A

181997789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49416611-G-C

http://identifiers.org/hco/4/GRCh38#181997889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49416515-A-C

181998174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49415944-T-C

181998562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49415752-G-C

181998838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49415481-T-C

181998956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49415392-A-T

181999098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49415271-A-G

181999227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49415156-G-A

181999301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49415086-G-A

182000534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49413545-T-C

182000690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49413079-T-A

182001060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49412665-G-T

182001157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49412563-A-T

182001347-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49412368-G-C

182001350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49412365-G-T

182001743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49411562-T-C

182002004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49409740-A-T

182002017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49409727-C-T

182002025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49409719-T-C

182002102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49409635-T-A

182002199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49409528-T-A

182002221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49409507-T-C

182002499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49409253-A-G

182002574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49409180-A-G

182002902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49408874-G-A

182003000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49408748-C-T

http://identifiers.org/hco/4/GRCh38#182003171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49408585-C-A

182003765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49408054-T-C

182003765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49408054-T-G

182004057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49407763-T-A

182004092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49407721-T-C

182010450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49407485-T-G

182010500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49407426-T-C

182010554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49407364-G-T

182010693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49407227-T-G

182010777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49407165-A-G

182010806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49407138-A-T

182011226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49406755-T-C

182011246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49406734-G-T

182011264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49406718-A-G

182011280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49406702-C-G

182011280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49406702-C-T

http://identifiers.org/hco/4/GRCh38#182011330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49406655-C-A

http://identifiers.org/hco/4/GRCh38#182013068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49406011-A-C

182013313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49405779-G-A

182013353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49405739-G-T

182013450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49405649-A-G

182013606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49405493-G-C

182013673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49405426-G-T

182013745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49405385-G-A

http://identifiers.org/hco/4/GRCh38#182014306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49405213-C-A

182014306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49405213-C-G

182014307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49405212-A-G

182014749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49404634-G-T

182015169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49404222-A-T

182015277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49404116-A-G

182015539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49403857-A-G

182015978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49403739-G-A

http://identifiers.org/hco/4/GRCh38#182016001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49403714-A-C

182016005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49403710-C-G

182016005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49403710-C-T

http://identifiers.org/hco/4/GRCh38#182016064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49403651-C-A

182016064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49403651-C-T

182016168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49403548-G-C

182016623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49403041-T-C

182016647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49403017-G-T

182016763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49402197-T-C

182016815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49402140-T-G

182017011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49401945-C-T

182017143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49401808-C-G

http://identifiers.org/hco/4/GRCh38#182017197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49401770-C-A

182017197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49401770-C-T

182017242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49401729-G-A

182017242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49401729-G-C

182017520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49401517-T-A

182017581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49401456-G-A

182018269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49400578-A-G

182018393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49400464-A-G

http://identifiers.org/hco/4/GRCh38#182018431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49400426-A-C

182018553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49400321-C-T

182022722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49397939-A-G

182022732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49397929-G-C

http://identifiers.org/hco/4/GRCh38#182022844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49397661-A-C

http://identifiers.org/hco/4/GRCh38#182022887-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49397618-A-C

182023151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49397328-A-G

182024107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49396345-G-C

182024107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49396345-G-T

http://identifiers.org/hco/4/GRCh38#182024119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49396333-A-C

182035576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49395486-T-C

http://identifiers.org/hco/4/GRCh38#182035580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49395482-C-A

182035755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49395337-G-A

182035803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49395289-C-T

182035866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49395229-C-T

182035965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49395128-C-G

182036515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49394576-C-G

182036515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49394576-C-T

182036848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49394262-A-G

182036946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49394172-G-A

182037119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49394009-A-T

182037537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49393863-G-C

182037560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49393841-A-G

182037620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49393771-T-C

182037679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49393712-A-G

182040593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49391224-A-G

182041049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49388993-A-G

182041049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49388993-A-T

182041529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49388401-C-T

182041999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49387898-C-T

http://identifiers.org/hco/4/GRCh38#182042119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49387803-C-A

182042119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49387803-C-G

182042686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49387238-C-T

182042801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49387119-G-A

182042956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49386988-C-T

182043155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49386791-T-C

182043163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49386783-T-C

182043176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49386770-A-G

182043585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49386369-A-G

182043676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49386259-G-A

182044033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49385983-G-A

182044206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49385819-G-A

182044206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49385819-G-C

182044408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49385630-T-C

182044576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49385243-C-T

182044659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49385037-T-C

182044681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49385015-G-A

182045181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49384527-G-A

182045307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49384377-T-C

182045396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49384289-A-T

182045581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49383726-G-A

182046795-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49382781-G-C

182046902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49382646-G-C

182046978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49382531-C-G

182046992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49382514-A-G

182047017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49382488-C-T

http://identifiers.org/hco/4/GRCh38#182047585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49382191-C-A

182047595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49382176-T-A

182047595-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49382176-T-G

182047609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49382162-G-A

182047609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49382162-G-T

182047936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49381844-G-T

182048012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49381768-T-C

182048140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49381672-C-T

182048195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49381620-C-T

182048310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49381514-A-G

182048360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49381458-C-T

182048591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49381229-C-T

182048656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49381119-A-G

182048714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49381058-A-G

182048842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49380929-T-C

182049424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49380347-G-A

182051718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49378990-T-G

182051784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49378924-A-G

182052177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49378386-G-A

182052346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49378228-G-A

182052359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49378215-T-C

182052436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49378179-C-T

182052458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49378156-G-A

182052879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49377817-C-T

182052900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49377796-T-C

182053145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49377713-T-C

182053247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49377611-T-C

182053484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49377373-C-G

182053484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49377373-C-T

182053492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49377365-T-C

182053688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49377161-T-G

182053940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49376907-C-T

182054093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49376774-C-G

182054251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49376621-C-G

182054931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49376290-C-T

182054945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49376263-C-T

182054959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49376249-G-A

182056159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49375227-C-T

182056304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49375108-G-A

http://identifiers.org/hco/4/GRCh38#182056541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49374843-C-A

http://identifiers.org/hco/4/GRCh38#182056601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49374782-A-C

182056630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49374638-A-G

182056634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49374634-T-G

182056911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49374341-C-T

182056968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49374284-T-C

182056997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49374255-C-T

182057017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49374235-T-C

182057797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49373643-T-C

182057797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49373643-T-G

182057814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49373625-C-T

182057963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49373474-A-G

182058412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49372727-T-C

http://identifiers.org/hco/4/GRCh38#182058418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49372721-C-A

182058530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49372649-T-A

182058530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49372649-T-G

182058669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49372516-G-A

182058671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49372514-A-G

182062528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49370802-C-T

182062569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49370747-A-G

182062626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49370684-T-C

182062946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49370254-G-A

182063079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49369926-T-C

http://identifiers.org/hco/4/GRCh38#182063156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49369849-C-A

182063156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49369849-C-G

182063429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49369575-T-C

182063737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49369275-G-A

http://identifiers.org/hco/4/GRCh38#182063865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49369142-C-A

182063869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49369138-A-G

http://identifiers.org/hco/4/GRCh38#182064027-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49369020-A-C

182064135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49368910-T-C

182065824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49368281-T-C

182066062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49368039-T-C

182066139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49367965-T-C

182066142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49367962-G-A

182066214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49366854-G-T

182066262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49366806-T-A

182066605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49366521-T-A

182066605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49366521-T-C

182067069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49366308-G-A

182067321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49366065-A-T

182067322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49366064-T-C

http://identifiers.org/hco/4/GRCh38#182067342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49366044-C-A

182067554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49365843-T-C

182067693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49365721-T-C

182067832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49365593-T-C

182068094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49365134-G-C

182068520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49363996-T-G

182068551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49363965-T-C

182069035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49363471-A-G

182069334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49363165-T-C

182069555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362947-A-G

182069555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362947-A-T

182069681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362820-G-A

http://identifiers.org/hco/4/GRCh38#182069714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49362775-C-A

182069746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362743-G-T

182069792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362701-G-A

182069792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362701-G-C

182069919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362608-G-A

182070006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362395-T-A

182070149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362242-G-A

182070149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362242-G-C

182070149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362242-G-T

182070235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362157-G-T

182070240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362152-G-A

182070240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362152-G-C

182070272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362121-C-T

182070474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49362023-G-C

182070660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49361964-G-A

182070728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49361893-G-A

182070847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49361764-T-C

182071006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49361588-T-C

182071006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49361588-T-G

182071074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49361464-T-A

182071074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49361464-T-C

182071094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49361445-G-A

http://identifiers.org/hco/4/GRCh38#182072730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49359557-C-A

http://identifiers.org/hco/4/GRCh38#182072933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49359349-A-C

182072933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49359349-A-G

182073671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49359012-G-A

182074128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49358522-T-C

182074286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49358114-A-G

182074350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49358046-T-C

182074353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49358043-A-T

182074520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49357861-T-G

182074593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49357788-T-C

http://identifiers.org/hco/4/GRCh38#182074781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49357618-A-C

182075035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49357289-G-T

182075498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49357131-G-A

182075805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49356825-G-A

182076507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49356719-C-T

182076538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49356685-C-G

182076538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49356685-C-T

182076812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49355880-G-A

182076812-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49355880-G-C

182076854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49355838-C-G

http://identifiers.org/hco/4/GRCh38#182076975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49355552-C-A

182076975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49355552-C-T

182077069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49355265-C-T

182077236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49355093-C-T

182077244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49355085-A-T

http://identifiers.org/hco/4/GRCh38#182077280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49355052-A-C

182077319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49355014-T-C

182077347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49354986-G-A

182077347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49354986-G-T

http://identifiers.org/hco/4/GRCh38#182077358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49354975-C-A

182078614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49354266-T-C

http://identifiers.org/hco/4/GRCh38#182078625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49354255-C-A

182079001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49353948-A-G

http://identifiers.org/hco/4/GRCh38#182079609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49353591-C-A

182079729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49353477-G-A

http://identifiers.org/hco/4/GRCh38#182079732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49353476-C-A

182079732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49353476-C-T

182079942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49353258-T-C

182080123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49353077-T-C

182080192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49353021-G-A

182080493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49352781-A-T

182080572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49352720-G-A

http://identifiers.org/hco/4/GRCh38#182081583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49351771-C-A

182081598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49351756-A-G

182081598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49351756-A-T

182081601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49351753-A-T

http://identifiers.org/hco/4/GRCh38#182081611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49351743-A-C

182081611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49351743-A-G

182081611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49351743-A-T

182081709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49351627-G-C

182081840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49351505-A-G

http://identifiers.org/hco/4/GRCh38#182082847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49350951-C-A

182082847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49350951-C-T

182082888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49350910-A-T

182083078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49350716-A-G

182083607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49350187-G-A

182083608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49350186-C-T

182083994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49349814-A-T

182084590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49349206-T-C

182084679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49349131-G-A

182084684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49349126-T-G

182084687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49349123-T-C

http://identifiers.org/hco/4/GRCh38#182084837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49348973-A-C

182084922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49348884-G-T

182085090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49348717-G-T

182085100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49348704-G-T

182085113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49348691-T-C

http://identifiers.org/hco/4/GRCh38#182085133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49348670-C-A

182085181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 49348620-G-T

182085201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49348600-G-A

182085439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49348350-T-G

182085797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49347987-T-C

182086097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49347695-G-C

182086417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49347397-T-C

182086576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49347306-G-A

182086576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49347306-G-T

182086856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49347025-G-A

182087042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49346673-C-T

182087204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49346530-A-G

182087489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49346213-T-A

182088068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49345625-A-G

182088217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49345413-A-G

182089003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49344739-A-G

182089151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49344644-T-A

182089172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49344623-G-A

182089172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49344623-G-T

182089582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49344353-A-T

182089666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49344266-C-T

182089963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49343959-A-T

182090131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49343834-T-C

182090612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49343354-A-G

182090654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49343315-A-G

182090670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49343288-A-G

182091119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49342878-A-T

182091507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49342368-C-G

182091507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49342368-C-T

http://identifiers.org/hco/4/GRCh38#182091838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49342068-A-C

http://identifiers.org/hco/4/GRCh38#182092032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49341880-A-C

182093103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49341461-A-G

182093359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49341238-A-T

182094040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49340572-G-A

182094076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49340536-C-T

182094162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49340438-G-A

182097131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49338236-T-C

182097672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49337510-C-T

182097673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49337509-G-A

182097799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49337327-G-C

http://identifiers.org/hco/4/GRCh38#182102256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49336513-A-C

182102765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49336012-G-A

182102924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49335859-C-T

182103004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49335795-C-T

182103030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49335780-T-C

182103990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49334800-A-T

182107548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49331630-C-T

182107779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49331404-T-C

182108036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49331143-G-A

182108120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49331043-T-A

182108416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49330798-T-C

182108474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49330735-A-G

182108888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49329763-C-T

182108990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49329662-A-T

182109197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49329365-T-C

182109362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49329196-A-G

182109537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49329041-A-G

182109584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49329008-T-C

182109585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49329007-G-C

http://identifiers.org/hco/4/GRCh38#182109592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49329000-A-C

182109808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49328801-T-C

182110254-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49328451-C-G

182110833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49328162-T-C

182110979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49328002-G-A

182111062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49327922-A-T

182111169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49327824-G-A

182111178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49327815-A-G

182111476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49327524-G-C

182111477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49327523-G-A

182111666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49327341-C-T

182111782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49326667-T-C

http://identifiers.org/hco/4/GRCh38#182111951-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49326029-A-C

182112879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49324480-T-C

182112923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49324436-T-C

182113220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49324152-T-C

182113235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49324144-T-C

182113237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49324137-G-T

182113375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49323995-G-C

182113743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49323628-G-A

182113763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49323608-G-T

http://identifiers.org/hco/4/GRCh38#182114191-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49323238-A-C

182114378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49323117-G-A

182114378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49323117-G-T

182114508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49323059-A-G

182114742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49322908-G-A

182115198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49322251-A-G

182115297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49322140-A-G

182115419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49322046-A-T

182115431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49322031-G-A

182115541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321933-A-G

182115663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321824-G-A

182115863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321612-C-G

182115871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321604-C-T

http://identifiers.org/hco/4/GRCh38#182115975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49321491-C-A

182115975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321491-C-G

182116030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321437-A-G

182116077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321377-T-C

182116077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321377-T-G

182116216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321184-G-T

182116223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49321177-A-G

182116844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320858-G-C

182116917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320796-A-G

182117021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320690-T-C

182117053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320660-T-C

182117092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320626-G-A

182117092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320626-G-C

182117240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320481-T-C

182117303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320419-C-T

182117430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320291-T-G

182117672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320098-C-T

182117706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49320064-A-G

182118346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49319181-G-A

http://identifiers.org/hco/4/GRCh38#182118347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49319180-C-A

182118401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49319132-A-G

182118645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318766-T-C

182118647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318764-T-G

182118833-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318578-T-A

182118976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318417-T-C

182118977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318416-G-T

182119024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318372-G-A

182119171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49318206-C-G

182119556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49317830-G-A

182119559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49317827-G-A

http://identifiers.org/hco/4/GRCh38#182119728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49317740-A-C

182119728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49317740-A-T

182120417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49317144-C-T

182125980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49316483-T-C

182125989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49316474-T-A

http://identifiers.org/hco/4/GRCh38#182126054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49316408-A-C

182127178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49314482-T-C

182128242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313326-T-C

182128337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49313217-T-A

182128669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49312978-G-A

182128669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49312978-G-T

182128786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49312849-C-G

182129285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49312359-T-C

182129684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49312006-T-G

182129789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311916-G-A

182129802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311903-A-G

182130349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311333-A-G

182130703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49311014-T-C

182131428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49310259-T-A

182131695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49310032-A-G

182131712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49310016-G-A

182131781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309943-T-G

182131838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309885-A-G

182131868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309855-A-G

182131872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309851-G-A

http://identifiers.org/hco/4/GRCh38#182131915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49309808-A-C

182132163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49309583-G-A

182133115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308858-C-T

182133297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308675-A-G

182133297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308675-A-T

182133417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308563-G-C

182133428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308554-T-G

182133535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308453-C-T

182133605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49308287-G-A

182133724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307948-C-T

182133928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49307743-T-C

http://identifiers.org/hco/4/GRCh38#182134326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49306715-A-C

182134326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49306715-A-G

182134974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305969-G-A

182135337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305810-G-A

182135481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305701-T-G

182135700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305454-G-A

182135700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49305454-G-T

http://identifiers.org/hco/4/GRCh38#182135920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49305246-A-C

182136252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49304917-T-C

182136466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49304691-C-G

182136493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49304663-C-T

182136540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49304617-G-T

182136791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49304343-A-G

http://identifiers.org/hco/4/GRCh38#182136952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49304046-C-A

182137102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49303899-G-C

182138123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302877-C-T

182138225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302726-C-T

182138352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302595-G-A

182138352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49302595-G-C

182138865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49302046-C-T

182139167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49301759-A-G

182139200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49301646-A-G

182139598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49301318-C-T

182140067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49300877-A-G

182140230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49300663-A-T

182140304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49300582-C-T

182140379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49300512-G-C

182140613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49300290-G-A

http://identifiers.org/hco/4/GRCh38#182140620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49300283-C-A

182140621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49300282-C-T

182140757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49300151-A-G

182140829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49300104-G-C

182141011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299957-T-C

182141011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299957-T-G

http://identifiers.org/hco/4/GRCh38#182141036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49299934-C-A

182141170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299873-A-G

http://identifiers.org/hco/4/GRCh38#182141182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49299861-C-A

182141478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299588-G-A

182141532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299465-G-A

182141532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299465-G-C

182141532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299465-G-T

182141543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299450-A-G

182141607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299366-G-C

http://identifiers.org/hco/4/GRCh38#182141655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49299286-C-A

182141655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299286-C-T

182141841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299097-G-A

182141841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299097-G-T

182141867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299071-A-G

182141877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299059-T-C

182141897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49299039-G-T

182141945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298982-G-A

182142115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298813-G-T

182142197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298748-T-C

182142236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298707-T-C

http://identifiers.org/hco/4/GRCh38#182142296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49298646-C-A

182142300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298642-G-A

182142382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298560-G-T

182142435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298506-G-A

182142435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298506-G-T

http://identifiers.org/hco/4/GRCh38#182142560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49298387-C-A

182142560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298387-C-T

182142585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298364-G-T

http://identifiers.org/hco/4/GRCh38#182142596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49298353-C-A

182142662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298302-C-T

182142708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298276-A-G

http://identifiers.org/hco/4/GRCh38#182142787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49298210-C-A

182142803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298194-A-G

http://identifiers.org/hco/4/GRCh38#182142830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49298158-C-A

182142830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298158-C-T

http://identifiers.org/hco/4/GRCh38#182142851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49298148-C-A

182142851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298148-C-T

http://identifiers.org/hco/4/GRCh38#182142852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49298147-C-A

182142852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298147-C-T

182142900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298100-G-T

182142902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298098-G-C

182142902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298098-G-T

182142947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298046-T-C

182142971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298020-G-A

182142971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298020-G-T

http://identifiers.org/hco/4/GRCh38#182142981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49298010-C-A

182142981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49298010-C-G

http://identifiers.org/hco/4/GRCh38#182143096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49297887-C-A

http://identifiers.org/hco/4/GRCh38#182143204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49297781-C-A

182143204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49297781-C-T

http://identifiers.org/hco/4/GRCh38#182143205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49297780-C-A

182143205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49297780-C-T

182143215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49297771-C-T

http://identifiers.org/hco/4/GRCh38#182143216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49297770-C-A

http://identifiers.org/hco/4/GRCh38#182143326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49297663-C-A

182143465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49297519-T-C

182143918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49297062-C-T

182144110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 49296861-A-G

http://identifiers.org/hco/4/GRCh38#182144134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#49296837-C-A

http://identifiers.org/hco/4/GRCh38#182144188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#49296780-C-A

182144188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49296780-C-T

http://identifiers.org/hco/4/GRCh38#182144205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#49296763-C-A

182144205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49296763-C-T

182144317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49296647-G-A

182144317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49296647-G-T

182144370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 49296597-T-C

182144445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49296537-G-C

182144542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49296433-C-T

http://identifiers.org/hco/4/GRCh38#182144627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49296373-C-A

182144630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296370-G-T

182144724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 49296281-G-A

182144841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296153-G-A

182144841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 49296153-G-T

182144856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49296122-G-T

182144914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49296038-T-C

182144921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49296031-T-C

182145114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49295837-G-A

182145114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49295837-G-T

http://identifiers.org/hco/4/GRCh38#182145115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49295836-C-A

182145115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49295836-C-T

http://identifiers.org/hco/4/GRCh38#182145209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49295742-C-A

182145209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49295742-C-T

http://identifiers.org/hco/4/GRCh38#182145211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#49295740-C-A

182145211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49295740-C-T

182145230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49295725-G-A

182145230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28076
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 49295725-G-T