102744371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46587965-G-A

102744371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46587965-G-T

102744385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46587979-G-A

102744385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46587979-G-T

102744524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46588109-G-A

102745253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46588783-T-A

102745253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46588783-T-C

102745538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589202-A-G

102745666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589327-G-T

102745761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589564-T-C

102745927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589730-T-C

102745951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589756-A-G

102746031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589820-A-T

102746097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589886-A-G

102746142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589919-G-A

102746173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589946-G-A

102746173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589946-G-C

102746213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589973-T-G

102746218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589978-T-C

102746219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589979-T-G

http://identifiers.org/hco/10/GRCh38#102746228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46589988-C-A

102746228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589988-C-T

102746238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46589998-G-A

102746242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46590003-C-T

102746267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46590031-A-G

102746379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46590146-C-T

102746399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46590166-T-G

102746499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46590265-T-C

102746552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46590323-A-G

102746608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46590372-T-C

102746610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46590374-G-T

102746704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46590420-G-A

102747468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46591089-T-C

http://identifiers.org/hco/10/GRCh38#102748449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46591558-C-A

102748466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46591575-C-T

102748674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46591758-A-G

102748885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46591944-G-T

102749016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46592045-G-A

102749098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46592124-A-G

102749239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46592259-T-C

102749283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46592316-G-A

102749283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46592316-G-C

102749432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46592430-G-A

102751131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46593797-G-C

102751146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46593812-A-G

102751151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46593817-C-T

102751204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46593967-G-A

102751285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46594073-T-A

102751294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46594082-G-A

102751322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46594110-C-T

102751343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46594130-G-A

102751343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46594130-G-C

102751343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46594130-G-T

102751498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46594245-G-C

102751550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46594291-T-C

102751648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46594381-T-A

102751688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46594421-C-T

102751779-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46594519-T-G

102751967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46594678-T-C

http://identifiers.org/hco/10/GRCh38#102751980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46594690-A-C

102752005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46594707-C-T

102752381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46595233-G-A

102752381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46595233-G-T

102752510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46595353-A-G

102752617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46595473-T-C

102752750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46595605-T-C

102752767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46595622-G-A

102753050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46595897-G-A

http://identifiers.org/hco/10/GRCh38#102753847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46596708-A-C

102753999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46596881-C-T

102754197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46597343-C-T

102762265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46601315-T-G

102762266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46601316-C-T

102762469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46601587-T-C

102762578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46601710-T-G

102762757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46601887-C-G

102762846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46601958-C-T

102762847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46601959-G-A

102762873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46601994-G-T

102764595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46604717-C-T

102764634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46604738-A-G

102764665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46604769-A-G

http://identifiers.org/hco/10/GRCh38#102764912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46605023-A-C

102764912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46605023-A-G

102764984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46605106-G-C

102767098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46606328-A-T

102769549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46607087-C-G

102769554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46607092-A-G

http://identifiers.org/hco/10/GRCh38#102769958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46607523-A-C

102769958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46607523-A-G

102769958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46607523-A-T

102769960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46607525-G-A

102770083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46607646-T-A

102770111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46607687-C-T

102770201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46607776-T-C

102770365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46607863-A-G

http://identifiers.org/hco/10/GRCh38#102770480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46607972-A-C

http://identifiers.org/hco/10/GRCh38#102770728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46608166-A-C

102771063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46608459-T-C

102771186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46608557-A-G

102772959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46608821-C-T

http://identifiers.org/hco/10/GRCh38#102773064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46608924-A-C

102773218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46609089-A-G

102773262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46609133-C-T

102773617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46609400-G-T

102773664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46609515-G-C

102773963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46609845-A-G

102774064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46609947-A-G

102774270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46610137-G-A

102774599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46610446-C-T

102774635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46610500-T-A

http://identifiers.org/hco/10/GRCh38#102774723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46610625-A-C

102774907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46610810-A-G

102775253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46610939-G-A

http://identifiers.org/hco/10/GRCh38#102775329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46611000-C-A

102775329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46611000-C-G

102775329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46611000-C-T

102775367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46611033-C-G

102775472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46611134-G-A

102775472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46611134-G-C

102775726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46611372-G-C

102775780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46611418-G-A

102775780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46611418-G-C

102775780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46611418-G-T

102776015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46611602-G-A

102776197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46611796-G-A

102776197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46611796-G-T

102776352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46611954-C-G

102776383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46611984-C-T

102776476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46612073-T-C

102776592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46612178-T-G

102776767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46612343-A-G

102777072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46612651-C-T

102778259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46613788-C-T

102778400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46613907-G-A

102778599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46614067-C-T

102778667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46614129-T-C

102778733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46614187-T-C

102778733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46614187-T-G

102780015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46614844-G-T

102780231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46615556-T-C

http://identifiers.org/hco/10/GRCh38#102780280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46615589-A-C

102780598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46615884-A-G

102780885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46616108-A-G

102781209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46616641-G-A

102781477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46616893-G-A

102781498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46616914-G-C

102781696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46617088-G-C

102781724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46617116-G-C

http://identifiers.org/hco/10/GRCh38#102781743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46617134-C-A

102781782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46617172-A-G

102781830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46617221-A-T

102781832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46617223-G-T

102781859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46617249-T-C

102781901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46617311-T-C

102782060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46617503-G-T

102783143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46618531-G-A

102783233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46618608-A-G

102783311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46618665-C-T

102783338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46618686-C-T

102783415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46618748-G-A

102783415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46618748-G-T

102783443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46618775-G-A

102783620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46618928-C-T

102784066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46619351-C-T

102784379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46619611-A-G

102784398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46619630-C-G

http://identifiers.org/hco/10/GRCh38#102785702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46621051-A-C

102785702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46621051-A-G

102785830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46621175-G-A

102785903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46621250-C-T

102785929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46621275-C-T

102786051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46621396-C-T

102786227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46621566-T-C

102786266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46621774-G-A

102787203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46622767-C-T

http://identifiers.org/hco/10/GRCh38#102787279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46622846-A-C

102787450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46623046-T-A

102787456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46623052-C-T

102787457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46623053-G-A

102787472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46623068-T-C

102787525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46623111-C-T

102787563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46623147-T-G

102791228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46627794-G-A

102791273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46627832-T-G

http://identifiers.org/hco/10/GRCh38#102791344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46627898-C-A

102791344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46627898-C-T

102791485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46628037-G-T

102792036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46628472-C-T

102792251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46628666-T-C

102792266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46628678-C-T

102792294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46628706-G-T

102794231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46629480-A-G

102795483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46630090-C-G

102795694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46630248-A-G

102795809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46630349-G-A

102796336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46630852-C-T

102796363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46630872-T-C

102796382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46630889-T-C

102796433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46630938-T-G

102796443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46630952-C-T

102796537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46631022-C-T

102796606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46631082-G-C

102796620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46631096-T-C

102796631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46631113-T-G

http://identifiers.org/hco/10/GRCh38#102797175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46632304-A-C

102797398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46632513-G-A

102797616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46632604-G-A

http://identifiers.org/hco/10/GRCh38#102797651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46632621-C-A

http://identifiers.org/hco/10/GRCh38#102797913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46632708-C-A

102797913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46632708-C-T

102797929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46632728-G-T

102798166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46632965-T-C

102798226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46633026-G-A

102798226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46633026-G-C

102798226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46633026-G-T

102798297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46633098-A-G

102798311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46633112-T-C

102799521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46633204-G-T

102799578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46633251-C-G

102799600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46633273-G-T

102800358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46633957-C-T

102800504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46634119-C-T

102800986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46634723-C-T

102801021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46634758-T-C

102801064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46634777-C-G

102801184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46634877-G-C

102801469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46635099-T-G

102801572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46635466-C-G

102803050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46636259-C-T

102803185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46636350-A-G

102809725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46640779-C-T

102809726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46640780-A-G

102809801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46640823-G-A

102809801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46640823-G-T

102809831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46640847-A-G

102809847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46640864-T-C

102810017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 46641037-A-G

102811496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46642001-T-C

http://identifiers.org/hco/10/GRCh38#102811922-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46642090-A-C

102812445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46642274-T-G

102812455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46642284-T-C

http://identifiers.org/hco/10/GRCh38#102812665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#46642474-A-C

102812665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 46642474-A-G

102812683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 46642495-A-G

102812745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 46642563-A-G

102812833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 46642654-T-C

102812962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 46642783-G-A

102812981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 46642802-A-G

102813052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 46642879-G-A

102813142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 46642969-C-T

102813196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 46643023-C-T

102813337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643164-G-T

102813360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643187-G-A

102813406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643231-G-A

102813406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643231-G-T

http://identifiers.org/hco/10/GRCh38#102813429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46643248-C-A

102813429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643248-C-T

http://identifiers.org/hco/10/GRCh38#102813479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46643295-C-A

102813546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643364-G-C

102813546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643364-G-T

http://identifiers.org/hco/10/GRCh38#102813588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46643391-A-C

102813588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643391-A-G

http://identifiers.org/hco/10/GRCh38#102813601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46643404-A-C

102813639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643442-G-A

102813639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643442-G-T

102813640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643443-T-A

102813650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643455-G-A

102813650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643455-G-T

102813697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643504-G-T

102813823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643603-G-A

102813823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643603-G-T

102813926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643689-T-C

102813926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643689-T-G

102814180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643902-G-A

102814180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643902-G-T

102814218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643940-C-G

102814218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46643940-C-T

102814247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46643969-G-A

102814293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46644014-T-C

http://identifiers.org/hco/10/GRCh38#102814350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#46644069-C-A

102814602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46644282-T-C

102814864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46644547-G-T

102814935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46644616-G-A

http://identifiers.org/hco/10/GRCh38#102815026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46644703-C-A

102815026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46644703-C-G

http://identifiers.org/hco/10/GRCh38#102815047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46644786-C-A

102815097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46644836-C-T

http://identifiers.org/hco/10/GRCh38#102815249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46644985-C-A

102815249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46644985-C-T

102815289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46645025-C-T

102815298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46645034-G-A

102815352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46645085-C-T

http://identifiers.org/hco/10/GRCh38#102815376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46645101-C-A

102815376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46645101-C-G

102815376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46645101-C-T

http://identifiers.org/hco/10/GRCh38#102815605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46645256-C-A

102815605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46645256-C-T

102815714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46645351-T-C

http://identifiers.org/hco/10/GRCh38#102815808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46645440-C-A

102815957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46645533-A-G

102815966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46645542-A-G

102815976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46645552-G-A

102815976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46645552-G-T

102816029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46645600-G-A

http://identifiers.org/hco/10/GRCh38#102816174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#46645737-C-A

102816472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46645991-T-C

102816545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46646049-G-T

102818864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46647020-C-T

102818919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46647072-A-G

102818923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46647076-C-T

102818934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46647087-A-G

102818983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46647337-G-A

102819235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46647575-C-T

102819249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 46647589-T-G

102821128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46648768-A-G

102821502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46648844-A-T

102821549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46648888-C-T

102821627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46648926-A-G

102822457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46649546-G-T

102822619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46649681-C-G

102822760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46649825-G-T

102826490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46652515-C-T

102827515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46652780-A-G

http://identifiers.org/hco/10/GRCh38#102827576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46652839-C-A

102827754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46653027-T-C

http://identifiers.org/hco/10/GRCh38#102830518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46655606-C-A

102830518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46655606-C-G

102830518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46655606-C-T

http://identifiers.org/hco/10/GRCh38#102830524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46655612-A-C

102830524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46655612-A-G

102830524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 46655612-A-T

102830567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46655653-G-A

102830567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 46655653-G-T

102830616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 46655692-G-A

102830616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 46655692-G-T

102830719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 46655781-C-T

http://identifiers.org/hco/10/GRCh38#102830786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46655848-C-A

102830786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 46655848-C-T

102831002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656065-G-A

102831002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656065-G-T

102831008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656071-G-A

102831008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656071-G-T

102831362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656301-G-C

102831362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656301-G-T

102831384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656323-G-T

102831394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656333-T-A

102831394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656333-T-G

102831438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656377-G-C

102831438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656377-G-T

102831456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656395-G-A

102831497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656436-G-C

102831515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 46656460-G-T

102831548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 46656493-G-A

102831548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 46656493-G-T

http://identifiers.org/hco/10/GRCh38#102831667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46656590-C-A

102831699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46656617-G-A

102831763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656680-A-G

102831804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656725-G-T

102831821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46656742-A-G

102832555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 46657155-G-A

102832555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 46657155-G-C

102832564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 46657164-G-A

102832778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46657375-T-C

102832817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46657413-G-A

102832851-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46657447-T-A

102832851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46657447-T-G

102832888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46657484-G-T

http://identifiers.org/hco/10/GRCh38#102832892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46657488-A-C

http://identifiers.org/hco/10/GRCh38#102832911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46657508-C-A

102832911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46657508-C-T

102832927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46657523-C-G

102832927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46657523-C-T

102833004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46657596-G-A

102833011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 46657603-G-A

102833076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46657668-T-C

102833082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46657674-T-A

102833113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46657705-G-T

102833212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 46657804-G-C

http://identifiers.org/hco/10/GRCh38#102833417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#46657985-C-A

102833417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46657985-C-T

102833963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46658092-G-T

102833988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46658118-G-T

102834016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46658141-T-C

102834399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46658497-G-T

102834468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46658569-G-A

102834468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23510
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46658569-G-T