55993483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94341221-T-C

55993583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94341320-G-A

55993587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94341324-A-G

55993588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94341325-C-T

55993678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94341439-T-C

55993735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94341543-G-A

http://identifiers.org/hco/16/GRCh38#55993804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94343203-C-A

55994064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94343414-C-T

55994121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94343472-G-T

http://identifiers.org/hco/16/GRCh38#55994125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94343476-C-A

55994197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94343554-T-C

http://identifiers.org/hco/16/GRCh38#55994235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94343589-A-C

55994428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94343744-G-A

55994429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94343745-C-T

55994529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94343831-C-T

55994549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94343855-T-C

55994866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344164-G-A

55994875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344173-G-A

55994885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344183-A-G

55994971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344262-G-A

http://identifiers.org/hco/16/GRCh38#55995095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94344399-C-A

55995165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344462-G-A

55995165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344462-G-T

55995224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344524-A-G

55995251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344552-C-T

http://identifiers.org/hco/16/GRCh38#55995271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94344570-A-C

55995369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344667-T-G

55995501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344785-A-G

55995519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344803-G-T

55995528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344812-C-G

55995528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344812-C-T

55995692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94344975-G-A

55995829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345089-A-G

55995854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345111-G-A

55995879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345136-A-G

http://identifiers.org/hco/16/GRCh38#55995892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94345138-C-A

55996162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345406-A-G

http://identifiers.org/hco/16/GRCh38#55996209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94345610-C-A

55996223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345653-A-T

55996325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345765-G-A

55996357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345803-G-A

55996474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94345912-A-T

http://identifiers.org/hco/16/GRCh38#55996586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94346022-C-A

55996586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94346022-C-T

55996645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94346084-G-T

55996882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94346357-C-T

55997298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94346706-G-A

56001220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94347435-A-G

56001264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94347466-T-C

56001290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94347490-T-G

56001450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94347643-G-A

56001600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94347759-G-A

56001894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94348030-G-A

56001895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94348031-T-A

56001895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94348031-T-C

http://identifiers.org/hco/16/GRCh38#56001975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94348111-A-C

56002143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94348261-C-G

56004120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94348660-G-T

56004185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94348709-A-G

56004320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94348844-C-T

56005233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94349874-G-C

56005472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94350080-G-T

56005473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94350081-C-T

56005956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94350579-C-T

56006011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94350628-G-A

56006701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94351778-A-G

56007006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94352059-G-A

56007062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94352119-G-A

56007062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94352119-G-T

56007278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94352293-G-A

56007290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94352305-C-T

56007376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94352390-T-G

56008047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94353060-G-A

56008313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94353289-G-A

56008314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94353290-A-T

56008334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94353309-C-T

56008364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94353339-G-A

56008409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94353383-G-A

56008409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94353383-G-T

56008904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94353821-C-T

56009081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94353974-A-G

56009147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94354036-T-C

56009280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94354168-C-T

56009536-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355101-T-A

56009590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355157-T-G

56009835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355391-T-C

56009990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355553-T-C

56010005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355568-T-A

56010413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355827-T-C

http://identifiers.org/hco/16/GRCh38#56010445-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94355849-A-C

56010512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355916-A-G

56010584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94355997-T-A

56010624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94356043-G-A

56010755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94356143-A-G

56010923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94356293-G-A

56010956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94356406-C-T

56011176-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94356862-T-A

56011358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94356993-G-A

56011433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357067-T-C

56011492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357109-T-C

56011694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357293-A-G

56011752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357335-T-C

56011973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357489-C-T

56012226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357756-C-T

56012257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357784-G-C

56012303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357831-T-C

56012316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94357844-C-T

http://identifiers.org/hco/16/GRCh38#56012443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94357944-C-A

56012578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358072-T-A

56012578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358072-T-C

56012578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358072-T-G

56012713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358188-C-T

56012877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358345-A-G

56012901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358367-C-G

56012901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358367-C-T

56012980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358512-A-T

56013043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358572-A-G

56013055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358584-C-T

56013211-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358742-T-A

56013224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358755-G-A

56013286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358802-C-T

56013369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358881-C-G

56013391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358900-A-G

56013469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94358978-T-C

56013503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359012-G-A

56013503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359012-G-T

http://identifiers.org/hco/16/GRCh38#56013543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94359053-C-A

56013543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359053-C-G

http://identifiers.org/hco/16/GRCh38#56013632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94359142-C-A

56014586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359514-C-T

56014779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359703-C-T

56014798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359719-T-C

56014859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359774-C-T

56014860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359775-A-G

56014885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359805-C-G

56014902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359821-A-G

56014950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94359875-A-G

56015625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363483-A-G

56015954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363796-G-T

56015963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94363805-A-T

56016303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364484-A-G

56016360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364541-A-G

56016366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364547-C-T

56016371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364552-G-C

http://identifiers.org/hco/16/GRCh38#56016428-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94364631-A-C

56016433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364636-T-C

56016437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364640-G-A

56016437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364640-G-T

56016476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364674-T-C

56016540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364734-G-A

56016561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364755-A-G

56016667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364831-G-A

56016727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94364875-C-T

56016950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94365043-C-T

http://identifiers.org/hco/16/GRCh38#56017111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94365198-C-A

56017117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94365204-C-T

56018124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94367918-A-G

56018229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94368018-A-G

56018620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94368379-G-A

http://identifiers.org/hco/16/GRCh38#56019088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94369229-A-C

56019095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94369236-C-G

http://identifiers.org/hco/16/GRCh38#56019096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94369237-C-A

56019178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94369324-T-C

56019263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94369385-T-C

56019676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94369786-C-T

56019717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94369829-G-A

56019717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94369829-G-C

56019949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370075-A-G

56020226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370312-T-C

56020246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370351-C-G

56020329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370435-C-T

56020395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370500-G-A

56020455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370556-T-C

56020667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370739-G-A

56020762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370828-G-A

56020871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370938-T-C

56020900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370967-T-C

56020900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370967-T-G

56020923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94370994-G-A

56021232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94371300-A-G

56021796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94371480-G-C

http://identifiers.org/hco/16/GRCh38#56022464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94372046-C-A

56022486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372068-A-G

56022486-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372068-A-T

56022714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372268-G-C

56022716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372270-G-T

56022782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372319-G-A

http://identifiers.org/hco/16/GRCh38#56022841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94372378-C-A

56022841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372378-C-T

http://identifiers.org/hco/16/GRCh38#56022870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94372407-C-A

56022883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372416-T-C

56022938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372440-C-T

56023112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372609-G-A

56023172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372670-G-A

56023190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372688-C-T

56023316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372822-C-T

56023327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372833-T-C

56023366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94372872-C-T

56023459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373024-A-T

56023513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373079-A-T

56023584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373126-A-T

http://identifiers.org/hco/16/GRCh38#56023601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94373141-C-A

56023685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373225-C-G

56023691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373231-A-G

56023742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373282-C-T

56023808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373345-T-C

56023849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373383-A-T

56023919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373451-C-T

56023922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373454-G-A

http://identifiers.org/hco/16/GRCh38#56025195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94373698-C-A

56025195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373698-C-T

56025218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373721-A-G

56025218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373721-A-T

56026329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94373909-A-G

56026458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94374025-G-T

56026668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94374230-G-C

56026845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94374434-T-C

56026845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94374434-T-G

56026847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94374436-G-T

56027092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94374682-T-C

56027190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94374774-A-G

56027300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94374894-G-A

56027414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94374970-A-G

56027482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94375033-C-T

56027702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94375229-G-A

56027740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94375288-T-G

56028169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94375716-G-T

56028262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94375802-A-G

56028706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94377429-T-C

http://identifiers.org/hco/16/GRCh38#56028946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94377644-C-A

56029146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94377832-A-G

56031155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94380957-T-C

56039829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94386776-A-T

56039897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94386837-C-T

56039972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94386898-A-G

56040010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94386938-G-A

56040503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387106-A-G

56040589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387188-C-T

56040664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387244-G-A

56040745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387360-A-T

56040776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387391-T-C

56040824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387438-G-A

56040925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387538-A-T

56040966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387579-G-A

http://identifiers.org/hco/16/GRCh38#56041220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94387822-A-C

56041220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94387822-A-G

56041508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94388126-G-A

56042035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94388628-G-A

http://identifiers.org/hco/16/GRCh38#56042099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94388678-C-A

56042099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94388678-C-T

56042328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94388901-G-T

56042559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94389092-T-C

56042737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94389277-G-A

http://identifiers.org/hco/16/GRCh38#56043732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94390238-C-A

56043733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94390239-T-C

56043772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94390291-T-A

56043798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94390317-G-A

56043798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94390317-G-C

56043815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94390334-T-C

56043944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94390576-C-T

56043952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94390584-T-A

http://identifiers.org/hco/16/GRCh38#56044499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94391308-C-A

http://identifiers.org/hco/16/GRCh38#56044501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94391310-A-C

56044513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94391319-C-T

56044591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94391394-G-T

56044611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94391413-C-G

56044633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94391433-T-C

http://identifiers.org/hco/16/GRCh38#56044920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94391661-C-A

56044983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94391714-A-G

http://identifiers.org/hco/16/GRCh38#56045401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94392328-C-A

56045401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94392328-C-T

56045539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94392609-G-A

56045667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94392734-G-A

56045960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94393642-C-G

56046012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94393693-C-T

56046069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94393749-T-C

56046179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94393869-G-A

56046200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94393889-A-G

56046283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94393964-G-C

56046284-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94393965-A-T

56046307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94393996-C-T

http://identifiers.org/hco/16/GRCh38#56046318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94394007-A-C

56046929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394276-A-G

56046929-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394276-A-T

56046930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394277-A-G

56046992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394320-G-T

56047173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394486-T-A

56047397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394671-G-A

56047397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394671-G-C

56047397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394671-G-T

56047401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394676-G-A

56047447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394689-T-C

56047483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394725-G-A

56047483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94394725-G-T

56047855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94395101-T-C

http://identifiers.org/hco/16/GRCh38#56048015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94395261-A-C

56048130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94395370-T-C

http://identifiers.org/hco/16/GRCh38#56048134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94395374-C-A

http://identifiers.org/hco/16/GRCh38#56048282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94395786-C-A

56048303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94395805-A-G

56048522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94396007-T-C

56048589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94396103-T-C

56048980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94396711-G-A

56048980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94396711-G-T

http://identifiers.org/hco/16/GRCh38#56049013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94396744-A-C

56049078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94396816-G-A

56049101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94396844-T-G

56049273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94397019-C-T

56051692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94400211-T-C

http://identifiers.org/hco/16/GRCh38#56051736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94400255-C-A

56051760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94400276-A-G

56051762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94400278-T-C

56051883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94400367-G-A

56052172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94400582-G-A

56052592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94401029-T-G

56052631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94401065-A-G

56052796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94401226-A-T

56052961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94401391-A-T

56053338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94401457-G-A

56053338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94401457-G-T

56054107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94401682-C-T

56054424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94401980-T-C

56054456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94402328-G-A

http://identifiers.org/hco/16/GRCh38#56054671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94402536-C-A

56054671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94402536-C-T

56055065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94402597-G-A

56055177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94402722-A-T

http://identifiers.org/hco/16/GRCh38#56056060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94404039-C-A

56056565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404828-G-A

56056565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94404828-G-C

56056924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94405160-G-C

56056948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94405189-T-C

56057013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94405241-G-A

56057032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94405260-G-A

56057422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94406722-A-G

56057495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94406795-T-C

56057559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94406858-C-G

56057622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94406920-A-G

56060249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94408966-T-C

56060280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94408997-A-G

56060589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409363-G-A

56060779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409523-A-T

56060929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409642-T-C

56061055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409771-G-C

56061189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94409874-C-T

56061629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94410281-A-T

56061763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94410347-G-A

56061764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94410348-G-T

56061766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94410350-G-A

56061766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94410350-G-T

56062244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94410573-A-G

56062300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94410624-G-C

56062399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94410742-T-C

56062664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94411014-A-G

http://identifiers.org/hco/16/GRCh38#56063610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94411847-A-C

http://identifiers.org/hco/16/GRCh38#56063815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94412507-A-C

56063848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94412538-G-A

56063946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94412656-G-A

56064028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94412739-A-G

56064028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94412739-A-T

56064029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94412740-T-C

http://identifiers.org/hco/16/GRCh38#56064530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94413264-A-C

56064824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94413956-A-G

56065084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414247-G-A

56065102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414265-A-G

56065330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94414591-A-G

56065535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414773-G-A

56065614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414852-A-G

56065758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94414996-C-T

56065911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94415155-G-T

56066199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94415446-C-T

56066462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94415691-A-G

56066465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94415694-G-A

56066715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94416003-T-A

56067027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94416315-T-C

56067039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94416327-A-G

56067439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94416729-G-A

http://identifiers.org/hco/16/GRCh38#56067626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94416915-C-A

56067626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94416915-C-T

56067956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417215-G-C

56067985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417238-T-A

56067985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417238-T-C

56068004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417252-C-G

56068099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417349-T-G

56068255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417478-C-T

56068494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417574-T-C

56068741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417814-A-G

56068870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94417918-T-C

56068985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94418022-G-A

56068985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94418022-G-T

http://identifiers.org/hco/16/GRCh38#56069067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94418098-C-A

56069070-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94418101-A-T

56069271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94418310-T-C

56069605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94419571-G-T

56069622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94419588-G-A

56069625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94419591-G-A

56069739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94419718-C-G

http://identifiers.org/hco/16/GRCh38#56070465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94420109-A-C

56070775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94420463-C-G

56070796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94420486-G-A

56071422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94420940-A-G

56071669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94421103-T-C

56071760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94421194-C-T

56071777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94421203-C-T

56071790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94421216-G-A

56071811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94421237-T-A

56071842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94421263-T-C

http://identifiers.org/hco/16/GRCh38#56072253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94421746-C-A

http://identifiers.org/hco/16/GRCh38#56072262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94421755-C-A

56072262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94421755-C-T

56072329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94421826-A-G

56072672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94422132-G-C

56072997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94422879-T-C

http://identifiers.org/hco/16/GRCh38#56073086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94422956-C-A

56073086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94422956-C-T

56073311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94423169-C-T

56073329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94423186-T-C

56073372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94423229-C-T

56073375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94423232-T-C

56073378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94423235-T-A

56073378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94423235-T-C

56073381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94423238-C-G

http://identifiers.org/hco/16/GRCh38#56073857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94424161-C-A

56073857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94424161-C-T

56073888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94424195-C-T

56073897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94424204-C-G

56073897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94424204-C-T

56074315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94424308-T-C

56074352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94424345-G-A

56074459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94424452-T-G

56074765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94424734-G-T

http://identifiers.org/hco/16/GRCh38#56075185-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94424930-A-C

56075307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94425079-C-T

56075400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94425183-G-C

56075593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94425466-C-T

56075599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94425472-G-A

56075599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94425472-G-C

56078118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429312-G-A

http://identifiers.org/hco/16/GRCh38#56078168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94429363-C-A

56078928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429656-G-A

56078928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429656-G-T

56079126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429841-T-C

56079255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429967-T-A

56079278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94429990-A-T

56079341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430052-T-A

56079341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430052-T-C

56079439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430139-T-C

56079452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430152-A-T

56079464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430164-G-A

56079490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430188-T-C

56079538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430236-G-C

56079566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430278-G-C

56079788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430516-C-T

56079852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430567-T-C

56080007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430704-T-C

56080108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94430796-G-A

56082932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94431231-G-T

56083026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94431338-T-C

56083224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94431523-A-G

56083385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94431593-C-T

56083730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94431937-G-A

56083787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94431994-A-G

56083795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94432002-C-T

56084477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94432470-T-C

56084646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94432649-T-C

http://identifiers.org/hco/16/GRCh38#56084695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94432696-A-C

56084820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94432821-T-C

56085176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433217-A-T

56085338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433598-T-A

56085342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433602-G-A

56085397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433658-C-T

56085502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433765-C-G

56085648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94433881-G-A

56086046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94434084-T-A

56086046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94434084-T-C

56086046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94434084-T-G

56086065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94434103-A-G

56086185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94434133-A-G

56086778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94434678-G-T

56087009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94435058-A-G

56087048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94435112-A-G

56087438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94435608-G-A

56087653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94435788-C-T

56087732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94435866-G-A

56088034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94436159-C-T

56088071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94436181-G-C

56088125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94436217-G-A

56088308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94436392-G-T

56088340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94436427-G-A

56088340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94436427-G-C

56088655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94437365-G-A

56088765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94437493-G-A

56088889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94437600-T-C

56088918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94437629-C-T

http://identifiers.org/hco/16/GRCh38#56089034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94437718-C-A

56089098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94437781-G-C

56089334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94438003-A-T

56089369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94438038-T-C

56089536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94438199-T-C

56089742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94438350-G-A

56089762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94438370-T-C

56089763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94438371-G-C

56089771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94438379-C-G

http://identifiers.org/hco/16/GRCh38#56090147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94438719-A-C

http://identifiers.org/hco/16/GRCh38#56090151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94438723-C-A

56090151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94438723-C-T

56090307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94438927-A-G

56090326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94438946-A-G

56090693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94439553-C-T

56090697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94439557-A-G

56090838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94439689-G-C

56090884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94439738-T-C

56091395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94439946-C-T

56091397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94439948-T-C

56091813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94440311-T-C

56092243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94440666-A-G

http://identifiers.org/hco/16/GRCh38#56092479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94440880-C-A

http://identifiers.org/hco/16/GRCh38#56092543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94440945-A-C

56098199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94445711-T-A

56098258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94445748-G-A

http://identifiers.org/hco/16/GRCh38#56098295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94445786-C-A

56098559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94446069-T-C

http://identifiers.org/hco/16/GRCh38#56098677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94446776-C-A

56098710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94446814-A-G

56098759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94446857-A-T

56098764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94446862-G-A

56098887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94446971-G-A

http://identifiers.org/hco/16/GRCh38#56098935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94447019-C-A

56099046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447144-G-T

http://identifiers.org/hco/16/GRCh38#56099193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94447238-C-A

56099347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447389-G-A

56099370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447412-T-G

56099385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447427-G-T

56099535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447559-G-A

56099543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447567-T-A

56099543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447567-T-C

56099653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447656-T-C

56099690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447693-G-T

56099703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447706-G-A

56099751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447750-G-T

56099854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447849-T-C

56099899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447888-G-A

56099909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447899-G-A

56099909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94447899-G-T

56100023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448020-A-G

56100023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448020-A-T

56100159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448133-G-A

56100183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448158-C-G

56100294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448266-A-G

56100613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448373-G-A

56100613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448373-G-C

56100829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448582-T-A

56100899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448649-G-A

56100899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448649-G-T

http://identifiers.org/hco/16/GRCh38#56100939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94448681-C-A

56100939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448681-C-G

56100951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448693-A-G

56100957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448699-A-G

56100992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448736-G-A

56100992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448736-G-T

56101036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94448779-C-T

56101643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94449001-G-A

56101738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94449083-G-A

56101739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94449084-C-T

http://identifiers.org/hco/16/GRCh38#56101756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94449097-C-A

56101756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94449097-C-T

56101887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94449213-G-A

56101984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94450326-A-G

56101999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94450340-T-C

56102012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94450353-C-T

56102014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94450355-G-T

56102137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94450467-T-G

56102138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94450468-A-G

56102190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94450520-G-T

http://identifiers.org/hco/16/GRCh38#56102210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94450531-C-A

56102310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94450632-C-T

56102378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94450698-C-T

http://identifiers.org/hco/16/GRCh38#56102388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94450713-C-A

56102411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94450736-A-G

56102411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94450736-A-T

http://identifiers.org/hco/16/GRCh38#56102620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94450953-C-A

56102669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94451003-C-T

56102864-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94451186-T-A

56102945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94451225-A-G

56102946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94451226-C-G

56102946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94451226-C-T

56103050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94451301-T-C

56103130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94451386-T-C

56103916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94451855-T-C

56104115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94452047-G-C

56104493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94452387-G-A

56104543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94452439-T-C

56104593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94452489-T-G

56104628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94452528-C-G

56104628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94452528-C-T

56104766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94452653-T-C

http://identifiers.org/hco/16/GRCh38#56105021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94452897-A-C

56105144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94453005-G-A

http://identifiers.org/hco/16/GRCh38#56105284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94453152-A-C

56105290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94453158-T-C

56105397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94453263-T-G

56105438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94453298-G-T

56105522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94453381-G-C

56105664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94453521-C-T

56105689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94453543-T-C

56105782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94453641-G-A

56105782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94453641-G-T

56106092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94453965-A-T

56106356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94454184-G-T

56106391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94454219-T-C

56106480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94454292-A-G

56106542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94454346-A-G

56106554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94454358-C-T

56106629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94454432-T-C

56106921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94454688-G-A

56107000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94454780-C-G

56107003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94454783-T-C

http://identifiers.org/hco/16/GRCh38#56107232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94455015-C-A

56107465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94455234-G-T

http://identifiers.org/hco/16/GRCh38#56107986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94455747-C-A

56108522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94456298-G-A

56108787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94456600-C-T

56108977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94456786-C-T

56108986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94456794-T-A

56109170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94457260-T-C

http://identifiers.org/hco/16/GRCh38#56109187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94457281-C-A

56109309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94457404-T-C

56109497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94457582-G-T

56109503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94457588-C-G

56109564-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94457651-T-A

56109739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94457855-A-G

56109794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94457912-C-T

56109941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94458055-G-T

56110016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94458116-G-T

56110017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94458117-C-T

56110158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94458270-T-G

56110310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94458427-T-C

56110343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94458446-A-G

56110594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94458671-G-A

56110668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94458744-C-T

56110702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94458778-T-C

56111355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94459482-G-T

56111438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94459557-G-A

56111487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94459605-T-C

56111755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94460905-G-A

http://identifiers.org/hco/16/GRCh38#56111795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94460943-A-C

56111802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94460950-C-T

56112129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94461273-G-A

56112191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94461335-G-A

56112341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94461473-A-G

56112437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94461568-G-A

56112482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94461614-T-C

56112865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94462007-T-C

56112889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94462022-C-G

56113303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94462426-A-G

56113304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94462427-G-T

56113363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94462482-T-C

56113424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94462544-C-G

56113469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94462589-C-T

56114048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94464351-G-A

56114076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94464379-C-T

56114128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94464526-A-G

56114135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94464533-A-T

56114146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94464544-A-G

56114261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94464650-C-T

56114369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94464741-C-T

56114541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94464895-A-G

56114877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94465129-C-T

56115062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94465311-T-C

56115220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94465630-T-C

56115588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94466002-T-A

56115627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94466042-C-T

56115844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94466487-G-A

56115905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94466533-C-G

56115933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94466560-T-C

http://identifiers.org/hco/16/GRCh38#56116265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94466878-A-C

56116276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94466889-C-T

56116338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94466951-T-C

56116360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94467015-C-T

56116571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94467222-C-T

56116634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94467272-G-A

56116816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94467454-A-G

56116902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94467534-T-C

56117231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94467917-A-G

56117498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94468197-C-T

56117825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94468596-C-T

56118246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94468860-G-A

56118332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94468936-A-G

56118379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94468981-T-A

56118379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94468981-T-C

56118379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94468981-T-G

56118396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94468998-A-G

56119348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94469218-T-C

56119493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94469352-C-T

56119537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94469402-T-C

56119537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94469402-T-G

56119596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94469455-G-A

56119822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94469683-G-A

56119822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94469683-G-T

56120253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94469976-T-C

56120321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94470041-G-A

56120330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94470050-G-T

56120460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94470192-T-A

56120756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94470500-A-G

56120947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94470660-G-A

56121265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94470962-G-T

56121301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94470998-T-C

56121307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94471004-T-C

56121611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94471534-A-T

http://identifiers.org/hco/16/GRCh38#56121633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94471556-C-A

56121652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94471575-G-A

56121652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94471575-G-T

56121671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94471594-A-G

56121671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94471594-A-T

56121742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94471643-C-T

56121798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94471690-C-G

56121798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94471690-C-T

56121942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94471839-G-T

http://identifiers.org/hco/16/GRCh38#56121975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94471851-C-A

56121979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94471855-G-A

56121979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94471855-G-T

http://identifiers.org/hco/16/GRCh38#56122016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94471892-C-A

56122019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94471895-G-T

56122109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94472002-C-T

56122323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94472187-T-C

http://identifiers.org/hco/16/GRCh38#56123046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94472444-C-A

56123321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94472943-G-A

56123407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94473017-C-G

56123749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94473500-T-C

56123806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94473559-G-T

http://identifiers.org/hco/16/GRCh38#56123808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94473561-C-A

56124193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94474130-T-C

56124276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94474212-G-T

56124376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94474307-G-A

56124408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94474338-G-A

56129942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94474999-T-C

http://identifiers.org/hco/16/GRCh38#56129994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94475051-C-A

56130001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94475058-G-A

56130004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94475061-G-A

56130009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94475066-A-G

56130065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94475117-A-G

56130214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94475266-A-T

56131074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94476294-A-G

56131153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94476372-T-C

56131223-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94476451-A-T

56131469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94476677-G-C

56131690-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94477016-G-C

56131748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94477073-T-C

56131749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94477074-G-A

56132049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94477344-T-A

56132273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94477559-C-T

56132294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 94477580-A-G

56132642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94477931-G-A

56132834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94478120-C-T

56133008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94478293-T-C

http://identifiers.org/hco/16/GRCh38#56133372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94478788-A-C

56133407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94478823-T-C

http://identifiers.org/hco/16/GRCh38#56134088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94481340-C-A

56134239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94481489-G-C

56134601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94481846-A-G

56134604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94481849-A-G

56134738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94481970-G-A

http://identifiers.org/hco/16/GRCh38#56135246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94482476-A-C

56135454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94482603-T-C

56135670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94482809-G-A

56135880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94483037-G-A

56135960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94483116-T-G

56136392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94483527-A-G

http://identifiers.org/hco/16/GRCh38#56136548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94483681-C-A

56136548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94483681-C-T

http://identifiers.org/hco/16/GRCh38#56136562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94483695-C-A

http://identifiers.org/hco/16/GRCh38#56136746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94483880-C-A

56136746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94483880-C-T

56136910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94484039-G-T

http://identifiers.org/hco/16/GRCh38#56137046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94484178-C-A

56137199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94484336-G-A

56137496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94484879-T-C

56138361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94485303-G-A

56138374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94485316-A-G

56138416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94485358-T-C

56138416-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94485358-T-G

http://identifiers.org/hco/16/GRCh38#56138467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94485400-A-C

56139124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94486130-C-T

56139236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94486240-T-C

56139779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94490333-A-G

http://identifiers.org/hco/16/GRCh38#56139990-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94490539-A-C

56140059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94490593-T-C

56140286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94490898-A-G

56140571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94491156-G-C

56140628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94491211-A-T

56140639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94491218-A-G

56141434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94491666-T-G

56142383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94491910-C-T

56142503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94492026-G-C

56142519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94492043-A-G

56142663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94492180-T-A

56143091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94492611-T-G

56149219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94493930-T-C

56149282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94494002-G-A

56149675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94494648-C-T

56149701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94494678-C-G

56149747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94494723-T-A

56150072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94494979-A-G

56150074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94494981-G-A

http://identifiers.org/hco/16/GRCh38#56150221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94495118-A-C

56150750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94495621-G-T

http://identifiers.org/hco/16/GRCh38#56150780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94495651-A-C

56150794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94495663-G-A

56150854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94495723-C-T

56151004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94495851-G-A

56151606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94496687-T-C

56151661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94496740-C-T

56151761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94496822-T-C

http://identifiers.org/hco/16/GRCh38#56151781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94496842-C-A

56151798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94496859-G-T

56151842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94496897-C-T

56151859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94496914-A-G

56152694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94498029-C-T

http://identifiers.org/hco/16/GRCh38#56152968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94498299-C-A

56154052-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94499435-T-A

56154105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94499475-T-A

56154198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94499568-C-T

56154209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94499579-G-C

56154479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94499829-C-T

56160915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94500065-G-C

56161095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94500261-G-A

56161281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94500435-G-T

56161678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94500981-C-G

56161678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94500981-C-T

56161781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94501088-G-A

56161899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94501206-C-G

56161935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94501242-T-G

56161994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94501259-C-T

56162030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94501295-T-G

56162332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94501553-G-C

http://identifiers.org/hco/16/GRCh38#56162521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94503518-C-A

56162796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94503999-G-C

56162858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94504062-A-G

56162969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94504161-T-A

56162994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94504181-A-G

56163011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94504198-C-T

56163379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94504570-G-A

56163631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94504827-A-G

56163682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94504875-T-C

56163841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94505024-T-A

56164060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94505249-A-G

56164307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94505468-T-C

56164354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94505515-T-A

56164567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94505692-G-A

56164612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94505741-T-C

56164629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94505754-C-T

56164654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94505820-G-T

56164695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94505861-A-G

56164760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94505928-G-A

56164795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94505959-A-G

56164815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94505979-G-A

56164849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94506011-G-A

56164907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94506069-T-A

56164981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94506146-A-G

56165607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94506251-T-G

http://identifiers.org/hco/16/GRCh38#56165934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94506522-C-A

56166729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94507160-G-C

56166841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94507271-T-C

56167229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94507837-G-C

56167472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94508059-C-T

56168426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94508502-G-A

56168565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94508643-C-T

56168894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94508978-G-A

56169092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94509398-T-C

http://identifiers.org/hco/16/GRCh38#56169775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94510078-C-A

56169807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94510109-G-C

56169814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94510116-T-C

56169945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94510402-T-C

56169945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94510402-T-G

56170598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94510435-A-G

56170636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94510467-T-C

56170809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94510634-A-G

56170987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94510796-G-A

56171066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94510872-G-A

56171337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94511164-A-T

56171505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94511343-A-G

56171582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94511411-T-C

56171607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94511436-C-T

56171614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94511442-T-A

56171627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94511452-A-G

56171804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94511641-G-A

56171929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94511678-G-T

56172162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94511787-G-A

http://identifiers.org/hco/16/GRCh38#56172179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94511805-C-A

56172271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94511913-C-T

56172302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94511944-C-T

56172307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94511949-A-G

56183024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94521793-G-A

56183094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94521865-T-C

56183094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94521865-T-G

56183203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94521930-T-G

56183603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94522334-C-T

56183644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94522380-G-A

56183644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94522380-G-T

56183875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94522593-T-C

56184310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94524265-C-T

56184380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94524329-G-A

56184600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94530609-A-G

56185168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94531129-G-A

56185489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94531446-T-C

56185536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94531550-G-A

56185536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94531550-G-T

56185553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94531566-C-T

56186212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94532410-T-C

56186238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94532434-G-A

56186239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94532435-C-T

56186615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94532895-C-G

56186636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94532915-C-G

56186636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94532915-C-T

56187067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94533302-A-T

56187165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94533408-C-T

56188435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94533590-G-A

56188435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94533590-G-T

http://identifiers.org/hco/16/GRCh38#56188833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94533943-A-C

56188954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94534059-C-G

56188954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94534059-C-T

56188979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94534084-G-A

56189105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94534703-G-A

56189407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94535206-G-A

56189560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94535405-G-T

56189732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94535589-C-T

http://identifiers.org/hco/16/GRCh38#56189976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94535821-C-A

56189976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94535821-C-T

56190053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94535893-T-C

56190187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536020-C-T

http://identifiers.org/hco/16/GRCh38#56190196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94536029-C-A

56190196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536029-C-T

56190217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536050-T-C

56190340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536172-G-C

56190340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536172-G-T

http://identifiers.org/hco/16/GRCh38#56190341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94536173-C-A

56190341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536173-C-G

56190386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536214-A-G

56190471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536316-T-C

http://identifiers.org/hco/16/GRCh38#56190621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94536437-C-A

56190621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536437-C-T

http://identifiers.org/hco/16/GRCh38#56190652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94536468-C-A

56190652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536468-C-T

56190663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536476-G-A

56190733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536547-C-T

56190792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536604-G-A

56190792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536604-G-T

http://identifiers.org/hco/16/GRCh38#56190868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94536664-C-A

56190868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536664-C-T

http://identifiers.org/hco/16/GRCh38#56190919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#94536719-C-A

56191008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536810-G-A

56191008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27543
most severe consequence: non coding transcript exon variant
orthologous variants: 94536810-G-T