170334197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70018387-A-G

170334261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70018451-G-T

http://identifiers.org/hco/2/GRCh38#170334443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70018583-C-A

170334472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70018612-T-C

170334502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70018642-G-A

http://identifiers.org/hco/2/GRCh38#170334515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70018655-C-A

170334515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70018655-C-T

http://identifiers.org/hco/2/GRCh38#170334826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70019321-C-A

170334826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70019321-C-T

170334896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70019391-A-T

170334900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70019395-A-G

170334900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70019395-A-T

170334931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70019426-T-G

170335227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70019715-G-T

170335270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70019758-G-T

170335360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70019856-G-T

170335550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70020046-A-T

http://identifiers.org/hco/2/GRCh38#170335570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70020062-A-C

170335570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70020062-A-G

170335570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70020062-A-T

170335610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70020102-C-T

170335625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70020117-A-G

http://identifiers.org/hco/2/GRCh38#170335932-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70020866-A-C

170335932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70020866-A-G

170335989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70020916-G-A

170336011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70020938-T-C

170336150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70021093-G-T

170336273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70021200-A-G

170336535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70021448-G-A

170336576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70021493-A-G

170336689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70021607-C-G

170336689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70021607-C-T

170336715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70021632-G-A

170336715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70021632-G-T

170336871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70021780-T-G

http://identifiers.org/hco/2/GRCh38#170336907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70021816-A-C

170336939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70021859-C-T

170337324-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70022323-C-G

170338856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70024459-G-A

170339379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70025616-C-T

170339644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70026078-T-A

170339752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70026209-G-C

170339886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70026343-C-G

170340290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70026716-A-G

170340433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70026840-T-C

170340478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70026883-A-G

170340505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70026910-A-G

170340724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70027127-G-A

170340881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70027232-T-C

170340923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70027276-G-A

170340923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70027276-G-C

http://identifiers.org/hco/2/GRCh38#170340961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70027305-C-A

170340961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70027305-C-T

http://identifiers.org/hco/2/GRCh38#170340967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70027311-C-A

170340967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70027311-C-T

170341002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70027346-T-C

170341204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70027512-G-A

170341410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70027715-A-G

170341437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 70027742-A-G

170341529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70027833-A-G

170341533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70027837-T-G

http://identifiers.org/hco/2/GRCh38#170341669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70027965-C-A

170341669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70027965-C-G

170341669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70027965-C-T

http://identifiers.org/hco/2/GRCh38#170344520-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70028131-C-A

http://identifiers.org/hco/2/GRCh38#170344540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70028146-C-A

170344574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 70028180-G-T

170344877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70028428-G-T

170344964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70028501-A-G

170344965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70028502-G-A

170344965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70028502-G-T

170345036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70028560-T-C

170345042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70028566-G-A

170345102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70028626-C-T

170345494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70028844-A-G

170345601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70028948-A-G

170345664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70028995-C-T

170346829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70029446-A-G

170347233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70029921-G-A

170353582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70031653-T-C

170353591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70031662-G-A

170353601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70031672-T-C

170353614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70031684-C-G

170353654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70031730-G-A

170353654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70031730-G-C

170353654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70031730-G-T

170353655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70031731-G-A

170353655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70031731-G-C

170353660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70031736-C-T

170354057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70032150-T-C

170354396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70032398-G-T

170354468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70032470-A-G

170354517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70032517-G-A

170354589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70032591-A-G

170355008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70032982-G-A

http://identifiers.org/hco/2/GRCh38#170355050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70033024-C-A

http://identifiers.org/hco/2/GRCh38#170355124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70033097-A-C

170355289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70033267-G-C

170355332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70033309-G-A

170355376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70033362-T-G

170355379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70033365-T-C

170355665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70033599-C-T

170355673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70033607-T-C

170355685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70033619-C-T

170355743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70033676-C-T

170355804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70033742-G-A

170355814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70033752-T-C

170357391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70033971-A-G

170357568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70034135-T-C

170357691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70034251-G-T

170357796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70034383-T-C

170358179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70034653-A-G

170358200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70034673-C-T

http://identifiers.org/hco/2/GRCh38#170358255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70034724-A-C

170358255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70034724-A-T

170358336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70034804-A-G

http://identifiers.org/hco/2/GRCh38#170358437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70034882-A-C

170358437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70034882-A-G

170358811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70035342-T-C

170358812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70035343-A-G

170359137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70035619-C-T

170359312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70035796-T-C

170359633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70036129-T-A

170359634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70036130-G-C

http://identifiers.org/hco/2/GRCh38#170359752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70036242-C-A

170359752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70036242-C-T

170359837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70036311-A-G

http://identifiers.org/hco/2/GRCh38#170359971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70036447-A-C

170360136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70036570-G-A

170360269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70036700-A-G

170360397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70036833-T-G

170360484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70036920-G-T

170360604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70037083-C-G

170360713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70037183-G-A

170360713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70037183-G-C

170360720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70037190-A-G

170360790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70037197-G-A

170360913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70037316-G-C

170360926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70037329-G-A

170360976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70037377-C-G

170360976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70037377-C-T

http://identifiers.org/hco/2/GRCh38#170361520-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70039588-A-C

170361520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70039588-A-G

170362695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70040660-C-G

170362820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70040756-T-C

170363216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70041152-A-G

170363400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70041336-C-T

170363497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70041476-G-A

170363712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70041681-T-G

170364115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70042080-C-G

170364179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70042152-G-A

170364237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70042238-G-T

170364375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70042629-A-G

170364383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70042637-C-T

170364735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70042945-T-C

170364840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70043053-C-T

170364857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70043070-A-G

170364874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70043087-T-C

http://identifiers.org/hco/2/GRCh38#170364898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70043497-A-C

http://identifiers.org/hco/2/GRCh38#170365217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70043787-C-A

170365352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70044537-A-G

170365366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70044550-G-T

170365618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70044779-C-T

170366775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70045154-T-C

170366810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70045188-A-G

170367451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70045751-C-T

http://identifiers.org/hco/2/GRCh38#170367495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70045779-A-C

170367997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70046255-G-A

170368008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70046266-C-T

170368166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70046410-T-C

170368705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70046876-A-G

170368709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70046880-A-G

170368718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70046890-G-A

170368930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70047064-G-C

170369074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70047211-A-G

http://identifiers.org/hco/2/GRCh38#170369075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70047212-C-A

170369075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70047212-C-T

170369101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70047237-A-G

170369155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70047289-C-T

170369164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70047298-T-G

170369209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 70047344-T-G

170369429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70047570-T-C

170369429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70047570-T-G

170369444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70047584-T-C

170369533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70047672-T-C

170369573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70047710-C-T

170369866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70048091-A-G

170369866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70048091-A-T

170370007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70048237-C-T

170371283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70049051-C-T

http://identifiers.org/hco/2/GRCh38#170371295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70049063-C-A

170371662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70049388-T-A

170371718-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 70049438-T-G

170371749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70049467-C-T

http://identifiers.org/hco/2/GRCh38#170371763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70049476-C-A

170371763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70049476-C-T

170373579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051335-G-A

170373609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051365-G-C

170373615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051371-G-T

170373659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051413-A-G

170373745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051496-G-A

http://identifiers.org/hco/2/GRCh38#170373756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70051507-A-C

170373756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051507-A-G

170373783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051534-C-T

170373979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051714-C-T

170373984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051719-G-A

170374010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051745-T-C

170374015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051750-G-C

170374046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051770-G-C

170374061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70051779-C-T

170374401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70052015-A-G

170374487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70052101-G-A

170374590-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053152-C-G

170374590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053152-C-T

170374602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053174-G-C

170374650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053222-G-C

170374661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053233-C-G

170374693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053262-C-G

170374881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053410-C-T

170374897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053426-T-C

170374949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053478-C-T

170375095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053601-G-A

170375095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053601-G-T

170375159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053661-A-G

170375262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053765-T-G

170375280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053783-G-A

170375321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053819-T-C

170375355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70053852-C-T

170375545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70054047-C-T

170375697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70054202-C-G

170375834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70054311-A-G

170375859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70054336-A-G

170376022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70054644-T-C

170376131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70054740-C-T

170376344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70054959-T-G

170376358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70054973-T-C

170376370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70054990-G-T

170376447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70055058-C-T

170376483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70055093-C-T

170376566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70055153-A-G

170376625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70055220-C-T

170376782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70055382-G-A

170377035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70055576-G-A

http://identifiers.org/hco/2/GRCh38#170377502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70055822-C-A

170377526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70055843-C-T

170377637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70055918-A-G

170377657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70055939-C-T

http://identifiers.org/hco/2/GRCh38#170377877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70056295-C-A

170377912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70057120-G-A

170378039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70057249-T-G

170378312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70057548-A-G

170378401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70057648-T-C

170378455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70057702-G-A

170378455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70057702-G-C

170378793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70058051-T-A

170381508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70061945-T-C

170381544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70061984-A-G

170381588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70062024-G-C

170381806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70062541-G-A

170381983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70062706-C-G

http://identifiers.org/hco/2/GRCh38#170381996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70062719-C-A

170381996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70062719-C-T

170382237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70063013-G-T

170382262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70063020-T-G

170382296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70063057-G-A

170382296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70063057-G-T

170382526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70063252-A-G

170382624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70063338-A-G

http://identifiers.org/hco/2/GRCh38#170383050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70063817-A-C

170383050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70063817-A-G

170383129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70063896-T-C

170383198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70063967-T-C

170383253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70064099-A-G

http://identifiers.org/hco/2/GRCh38#170383284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70064130-C-A

http://identifiers.org/hco/2/GRCh38#170383304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70064176-C-A

170383304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70064176-C-G

170383304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70064176-C-T

170383335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70064207-G-C

170383335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70064207-G-T

170383542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70064560-T-C

170383622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70064623-A-T

170383677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70064679-G-A

http://identifiers.org/hco/2/GRCh38#170383858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70064863-C-A

170383919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 70064930-G-A

170383919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 70064930-G-T

170384034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70065022-A-G

170384034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70065022-A-T

170385403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70067184-G-A

170385692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70067473-T-C

http://identifiers.org/hco/2/GRCh38#170385751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70067529-C-A

170386000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70067959-A-G

170386100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068054-T-A

170386100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068054-T-C

http://identifiers.org/hco/2/GRCh38#170386109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70068063-C-A

170386125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068079-A-G

http://identifiers.org/hco/2/GRCh38#170386135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70068102-C-A

170386200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068172-C-T

http://identifiers.org/hco/2/GRCh38#170386227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70068199-A-C

http://identifiers.org/hco/2/GRCh38#170386288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70068260-C-A

170386311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068283-T-C

170386316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068288-C-T

170386397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068366-T-C

170386659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068629-G-C

170386661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068631-T-G

170386707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068732-T-C

http://identifiers.org/hco/2/GRCh38#170386724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70068749-A-C

170386893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068918-C-T

170386958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068974-T-A

170386958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068974-T-C

170386969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068985-G-A

170386969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70068985-G-T

170387041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70069040-G-A

170387041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70069040-G-T

http://identifiers.org/hco/2/GRCh38#170387050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70069049-C-A

170387126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70069121-A-G

170387333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70069328-G-A

170387358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70069360-G-A

170387400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70069400-T-A

170387400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70069400-T-C

170387526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70069756-G-A

170387776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70070540-C-T

170387906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70070666-C-G

170387916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70070674-T-C

170388198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70070815-G-A

http://identifiers.org/hco/2/GRCh38#170388219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70070836-C-A

170388219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70070836-C-G

170388229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70070846-C-T

170388230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70070847-G-A

170388230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70070847-G-C

170388336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70070947-T-G

170388357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70070968-G-A

170388440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70071436-G-A

170388469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70071458-A-G

170388474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70071463-T-G

170388496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70071472-A-G

170388697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70071641-T-C

170388864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70071846-T-C

170388866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70071848-G-A

170388871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70071853-A-G

170388950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70071937-T-C

http://identifiers.org/hco/2/GRCh38#170390619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70074173-A-C

170390785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70074323-C-T

170390944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70074463-T-C

170391204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70074883-C-G

170391326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70075002-T-G

170391488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70075148-T-C

170391653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70075351-T-C

170391657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70075355-T-C

http://identifiers.org/hco/2/GRCh38#170391703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70075402-C-A

170391703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70075402-C-T

170391748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70075444-A-G

170391748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70075444-A-T

170391849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70075535-C-T

170392442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70075699-A-G

170392498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70075755-A-G

170392500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70075757-G-A

170392502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 70075759-G-A

http://identifiers.org/hco/2/GRCh38#170392528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70075794-C-A

170392528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70075794-C-T

170392719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70076046-A-G

170392767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70076089-G-A

170393493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70076508-A-T

170393501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70076516-A-G

170393569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70076586-G-A

170393589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70076606-G-T

170393665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70076681-T-A

170393868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70076885-A-G

170393885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70076899-G-A

170393977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70076984-G-A

170394006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70077022-C-T

170394052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70077066-G-A

170394063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70077077-A-G

170394455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70077630-T-C

170394577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70077742-A-G

http://identifiers.org/hco/2/GRCh38#170394745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70078100-A-C

170394745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70078100-A-G

170394785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70078139-T-G

170395039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70078408-C-T

170395317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70078678-T-C

170395449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70078804-G-A

170395480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70078835-A-T

170395688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70078991-G-A

170395736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70079039-G-A

170395829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70079110-G-A

170396027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70079237-C-T

170396241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70079419-G-A

170396252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70079426-T-G

170396553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70079703-T-C

170396553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70079703-T-G

170396640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70079789-T-G

170396670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70079819-G-A

170396785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70079936-T-C

170396871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70079988-G-T

170396966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70080082-A-G

170397348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70080472-A-G

170397804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70080922-T-C

170397841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70080949-C-T

170399898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70081795-T-C

170399900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70081797-C-T

170399946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70081843-C-T

170399952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70081849-C-T

170399955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70081852-G-A

170400052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70081948-G-A

170400052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70081948-G-T

170400061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70081957-G-T

170400066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70081959-G-T

http://identifiers.org/hco/2/GRCh38#170400075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70081966-A-C

170400075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70081966-A-T

http://identifiers.org/hco/2/GRCh38#170400118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70082011-C-A

170400146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70082039-C-T

170400217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70082110-T-C

170400217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70082110-T-G

170400305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70082198-T-A

http://identifiers.org/hco/2/GRCh38#170400356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70082242-C-A

170400356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70082242-C-T

170400357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70082243-G-A

170400369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70082273-G-A

170400369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70082273-G-T

170401322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70083152-G-T

170401590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70083424-T-C

170401703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70083556-G-A

170401703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70083556-G-C

170401703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70083556-G-T

170401773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70083612-T-A

170401776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70083615-T-G

170401921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70083646-G-A

170402013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70083687-T-C

170402041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70083712-G-T

170402086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70083743-C-T

170402088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70083745-G-C

170402110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70083767-G-A

170402436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70084318-C-G

170402444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70084326-A-G

170402621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70084549-A-G

170402711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70084616-A-G

170402808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70084701-T-A

http://identifiers.org/hco/2/GRCh38#170402832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70084723-C-A

170402832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70084723-C-G

170402832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70084723-C-T

170402879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70084768-T-C

170402879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70084768-T-G

170402887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70084776-C-T

170402977-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70084866-T-A

170402977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70084866-T-C

http://identifiers.org/hco/2/GRCh38#170403087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70084994-A-C

170403087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70084994-A-G

http://identifiers.org/hco/2/GRCh38#170403088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70084995-C-A

http://identifiers.org/hco/2/GRCh38#170403125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70085030-C-A

170403125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085030-C-T

http://identifiers.org/hco/2/GRCh38#170403138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70085047-C-A

170403138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085047-C-T

170403139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085048-T-A

170403157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085081-G-A

170404096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085447-A-G

http://identifiers.org/hco/2/GRCh38#170404128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70085476-C-A

http://identifiers.org/hco/2/GRCh38#170404134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70085482-C-A

http://identifiers.org/hco/2/GRCh38#170404216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70085562-C-A

170404216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085562-C-T

http://identifiers.org/hco/2/GRCh38#170404229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70085573-C-A

http://identifiers.org/hco/2/GRCh38#170404234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70085578-C-A

http://identifiers.org/hco/2/GRCh38#170404282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70085626-C-A

170404282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085626-C-T

170404433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085772-T-G

170404468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085795-G-A

170404468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085795-G-T

http://identifiers.org/hco/2/GRCh38#170404471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70085805-C-A

170404471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085805-C-T

170404488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085822-T-G

170404513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085847-T-G

http://identifiers.org/hco/2/GRCh38#170404517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70085851-A-C

170404517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085851-A-G

170404517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085851-A-T

170404518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085852-G-A

170404518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70085852-G-T

170404623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70086171-C-T

170404649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70086197-T-C

170404677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70086218-T-C

170404712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70086267-T-C

170404723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70086278-A-G

http://identifiers.org/hco/2/GRCh38#170405694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70086968-C-A

170405694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70086968-C-T

http://identifiers.org/hco/2/GRCh38#170405783-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70087038-A-C

170405783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70087038-A-G

170405783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70087038-A-T

170406002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70087205-G-A

170406002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70087205-G-C

170406013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70087215-T-G

170406023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70087225-T-C

170406846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70087826-C-T

http://identifiers.org/hco/2/GRCh38#170406937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70087913-A-C

http://identifiers.org/hco/2/GRCh38#170407031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70087979-C-A

170407568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088148-T-A

170407568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088148-T-C

170407568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088148-T-G

170407622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088212-G-A

170407622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088212-G-C

170407622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088212-G-T

170407650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088240-T-A

170407652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088242-G-A

170407652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088242-G-T

170407694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088287-C-T

170407695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088288-G-A

170407695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088288-G-C

170407695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088288-G-T

170407778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088370-G-A

170407893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088473-C-G

170407893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088473-C-T

170407906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088486-C-T

170407935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70088515-G-A

http://identifiers.org/hco/2/GRCh38#170408040-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#70089103-A-C

170408067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70089138-C-T

170408394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40713
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70089412-T-C