116085099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092001-T-C

http://identifiers.org/hco/5/GRCh38#116085111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47092013-C-A

116085111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092013-C-G

http://identifiers.org/hco/5/GRCh38#116085138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47092033-C-A

116085138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092033-C-G

116085201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092093-G-T

116085204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092096-G-A

116085204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092096-G-T

116085223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092110-G-A

116085223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092110-G-C

116085223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092110-G-T

116085228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092115-G-A

116085228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092115-G-C

116085228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092115-G-T

http://identifiers.org/hco/5/GRCh38#116085238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47092128-C-A

116085238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092128-C-G

116085238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092128-C-T

http://identifiers.org/hco/5/GRCh38#116085240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47092130-A-C

116085240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092130-A-G

116085240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092130-A-T

http://identifiers.org/hco/5/GRCh38#116085243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47092133-C-A

116085243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092133-C-T

116085244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092134-T-C

116085244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092134-T-G

116085256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092143-G-A

116085256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092143-G-T

116085269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092154-T-G

116085285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092170-T-C

116085285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092170-T-G

116085289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092174-G-A

116085289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092174-G-T

http://identifiers.org/hco/5/GRCh38#116085333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47092203-C-A

116085333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092203-C-G

116085333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092203-C-T

116085371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092252-G-A

116085371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092252-G-C

http://identifiers.org/hco/5/GRCh38#116085375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47092256-C-A

116085375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092256-C-G

116085438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092329-G-A

116085438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47092329-G-T

116085483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47092365-G-A

116085483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47092365-G-C

116085483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47092365-G-T

116085484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47092366-T-C

116085520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47092398-T-G

116085530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47092408-G-A

116085530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47092408-G-T

http://identifiers.org/hco/5/GRCh38#116085819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47092875-A-C

116085840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47092896-T-C

116087163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093177-A-G

http://identifiers.org/hco/5/GRCh38#116087380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47093383-C-A

http://identifiers.org/hco/5/GRCh38#116087422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47093421-C-A

http://identifiers.org/hco/5/GRCh38#116087430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47093429-C-A

http://identifiers.org/hco/5/GRCh38#116087432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47093431-A-C

116087432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093431-A-G

116087432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093431-A-T

http://identifiers.org/hco/5/GRCh38#116087462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47093453-C-A

116087462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093453-C-T

116087483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093473-A-G

116087506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47093492-A-G

116087528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47093514-A-G

116087584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47093570-G-A

116087601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093587-T-C

116087645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093629-T-A

116087689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093671-T-C

116087711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093693-G-C

116087730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093711-T-C

116087730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093711-T-G

116087735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093716-G-A

116087735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093716-G-C

116087735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093716-G-T

116087812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47093790-G-A

116088162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47094606-A-G

116088162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47094606-A-T

http://identifiers.org/hco/5/GRCh38#116088307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47094747-A-C

116088307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47094747-A-T

116090434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47096060-T-C

116090470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47096094-A-G

116090487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47096111-T-G

116090512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47096134-G-A

http://identifiers.org/hco/5/GRCh38#116090592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47096209-C-A

116090613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47096229-G-A

116090922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47096612-A-G

116091059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47096710-G-A

116091059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47096710-G-T

116091102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47096750-A-G

116091105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47096753-G-A

116091105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47096753-G-C

116091105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47096753-G-T

http://identifiers.org/hco/5/GRCh38#116091160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47096808-C-A

116091160-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47096808-C-G

116091160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47096808-C-T

116091244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47096881-T-C

116091251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47096888-G-T

116091254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47096891-A-G

116091406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47097069-A-G

116091775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47097475-T-C

116091777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47097477-G-A

http://identifiers.org/hco/5/GRCh38#116091927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47097774-C-A

116091927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47097774-C-T

116091958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47097805-A-G

116092559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47100821-T-C

116092594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47100856-A-G

116092594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47100856-A-T

116092606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47100868-G-A

116092606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 47100868-G-C

116092643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47100905-T-C

116092682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47100944-A-G

http://identifiers.org/hco/5/GRCh38#116092753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47101004-A-C

116092753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47101004-A-G

116096304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47103305-G-A

116096381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47103373-G-T

116096387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47103378-C-T

116096842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47104230-C-T

116115611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47107254-G-A

http://identifiers.org/hco/5/GRCh38#116115669-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47107300-A-C

116115679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47107310-C-T

116115714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47107344-C-T

116116038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47107664-G-A

116116102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47107735-C-T

http://identifiers.org/hco/5/GRCh38#116117614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47108438-C-A

116117614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47108438-C-G

116117614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47108438-C-T

http://identifiers.org/hco/5/GRCh38#116117662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47108522-C-A

116117662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47108522-C-T

116117708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47108559-T-C

116117709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47108560-G-T

116117878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47108636-C-T

116117912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47108669-T-G

http://identifiers.org/hco/5/GRCh38#116117938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47108679-C-A

116118049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47108783-C-T

116118120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47108841-G-A

116118166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47108894-G-A

116118346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47109028-A-G

116118415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47109096-T-C

116118507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47109206-G-T

116118538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47109238-A-G

116119285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47109972-G-A

116119430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47110114-G-A

116128059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47113911-A-T

116128669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47115611-T-A

116128731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47115665-A-G

116128731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47115665-A-T

116128842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47115779-A-G

116130498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47119344-G-A

116130889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47120167-A-T

116130995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47120273-A-G

116131023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47120300-A-G

116131078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47120353-A-G

116131125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47120387-A-G

116131371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47120650-C-T

116131487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47120736-C-G

116131524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47120776-T-C

116131527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47120779-C-T

116131572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47120823-T-C

116131638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47120882-G-C

116131740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47120978-A-G

116131822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47121059-A-T

116132142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47121241-T-G

116132143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47121242-G-C

116132211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47121296-A-G

116132398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47121437-G-A

116132663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47121591-A-G

116132748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47121617-G-C

http://identifiers.org/hco/5/GRCh38#116132752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47121621-C-A

116132771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47121640-A-G

116132916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47121752-A-G

116132977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47121797-A-G

116132981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47121803-A-G

116133008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47121830-A-G

http://identifiers.org/hco/5/GRCh38#116133081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47121897-C-A

116133180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47121998-G-T

116133187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47122005-A-G

116133187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47122005-A-T

116133210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47122017-A-G

116133243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47122056-T-G

http://identifiers.org/hco/5/GRCh38#116133318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47122109-A-C

116133493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47122278-T-C

116133617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47122431-A-G

116133968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47123447-G-T

116134005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47123484-T-C

116134014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47123493-A-T

116134235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47123713-T-C

116134292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47123747-A-G

116134429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47123807-T-C

116134498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47123902-G-A

116134498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47123902-G-C

116134810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124006-A-G

116134810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124006-A-T

116134953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124049-T-G

116135003-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124100-T-A

116135005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124102-C-G

116135045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124139-T-C

116135067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124159-C-T

116135074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124166-T-C

116135358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124434-C-G

116135404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124477-T-G

116135410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124483-A-G

116135410-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124483-A-T

116135907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124738-A-G

116136101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47124849-T-A

116136358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47125090-A-G

116136386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47125109-C-T

116136426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47125143-C-G

http://identifiers.org/hco/5/GRCh38#116136693-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47125391-A-C

116136693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47125391-A-G

116136759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47125459-T-G

116136770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47125474-A-G

116136776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47125480-A-G

116136947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47125617-G-A

116136947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47125617-G-T

116137009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47125672-C-G

116137100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47125759-C-G

116137100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47125759-C-T

116137599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47126219-G-C

116137606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47126225-T-G

116137705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47126305-C-T

http://identifiers.org/hco/5/GRCh38#116137722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47126323-C-A

116137822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47126425-G-T

116137966-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47126572-T-G

116138038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47126644-T-C

116138702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47127237-A-G

116138709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47127244-G-A

116138735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47127269-G-A

116138739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47127273-T-C

116138751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47127285-A-G

116138801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47127331-T-C

116138824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47127353-T-C

116139005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47127619-A-G

http://identifiers.org/hco/5/GRCh38#116139100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47127719-A-C

116139136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47127754-G-A

116139410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47128042-A-G

116139661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47128283-C-T

116152768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47135276-G-A

116152786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47135295-G-A

116152987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47135481-A-G

116153555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47136237-A-G

http://identifiers.org/hco/5/GRCh38#116153609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47136286-A-C

116153640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47136314-C-G

http://identifiers.org/hco/5/GRCh38#116153659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47136333-C-A

116153730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47136404-G-A

116153875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47136558-G-T

116155106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47136950-A-G

116155150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47136988-A-T

116155185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47137022-G-A

116155385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47137226-A-G

116155397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47137242-A-G

116155451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47137295-A-G

116155486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47137320-T-C

116155668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47137513-A-G

116155668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47137513-A-T

116155720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47137564-C-G

116155734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47137634-T-C

116155734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47137634-T-G

116155777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47137739-C-G

116155954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47137905-G-A

116156015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47137968-T-C

116156102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47138064-C-G

116156108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47138070-C-T

116156158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47138125-G-T

116156161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47138128-C-G

116156248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47138217-A-G

116156250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47138219-A-G

116156288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47138254-G-A

116156306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47138269-G-A

116156306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47138269-G-T

http://identifiers.org/hco/5/GRCh38#116158684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47141754-A-C

http://identifiers.org/hco/5/GRCh38#116158793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47141848-A-C

116158793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47141848-A-G

116158810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47141858-T-G

116158882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47141925-A-T

116158946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47141983-A-G

116158968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47142005-C-T

116159020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47142055-A-G

116159026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47142061-A-T

116159067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47142102-T-G

116159175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47142209-C-T

116159277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47142311-T-C

116159280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47142314-C-G

116159282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47142316-A-G

116159374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47142408-T-G

116159492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47142514-T-G

116162035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47135276-G-A

116162035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47135276-G-T

116162052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47135295-T-G

116162056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47135299-A-G

116162530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47135541-G-A

116177567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47146310-C-T

116177625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47146365-G-T

116178182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47146970-A-G

116178301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47148012-G-A

116178381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47148092-A-G

116178422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47148126-C-T

116178529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47148242-T-C

116178813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47148519-G-A

116178826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47148532-C-G

http://identifiers.org/hco/5/GRCh38#116179155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47148844-A-C

http://identifiers.org/hco/5/GRCh38#116179248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47148957-A-C

116179248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47148957-A-G

116179264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47148973-T-C

116179267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47148976-A-T

116179289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47149002-G-A

116179371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47150630-C-T

http://identifiers.org/hco/5/GRCh38#116179393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47150652-C-A

116179581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47150841-G-A

116179608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47150867-G-A

116179658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47150890-T-A

116179658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47150890-T-G

116179803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47151001-T-A

116179803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47151001-T-C

116179923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47151113-A-G

116179995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47151163-G-T

116180158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47152154-G-A

116180158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47152154-G-T

116180235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47152233-A-G

116180249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47152245-G-A

116180389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47152363-A-G

116180395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47152369-T-G

116184488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47152904-C-T

http://identifiers.org/hco/5/GRCh38#116184587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47153005-C-A

116184619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47153031-C-G

116184847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47153240-A-G

http://identifiers.org/hco/5/GRCh38#116184937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47153324-A-C

116184982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47153367-T-C

http://identifiers.org/hco/5/GRCh38#116185085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47153472-A-C

116185085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47153472-A-G

116185199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47153581-A-G

116185460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47153830-A-G

116185584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47153943-C-T

116185595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47153954-C-G

116185612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47153971-A-G

http://identifiers.org/hco/5/GRCh38#116185708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47154035-A-C

http://identifiers.org/hco/5/GRCh38#116185709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47154036-C-A

116187169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47155133-G-C

116187193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47155156-C-T

116187378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47155328-C-G

116187488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47155837-T-C

116188222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47156507-G-A

116190159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47157571-C-G

116190173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47157585-A-G

116190454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47157623-A-G

116190517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47157680-C-T

116190575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47157738-G-A

116196765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47161596-A-T

116197234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47162714-A-G

116197768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47163113-A-G

116198003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47163360-T-C

116198095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47163445-T-C

116198098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47163448-A-G

http://identifiers.org/hco/5/GRCh38#116198102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47163452-C-A

116204321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47164286-A-G

116204326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47164291-C-G

116204344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47164309-A-G

116204535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47164487-T-C

116204587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47164545-C-G

116204710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47164650-A-G

116204731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47164671-C-T

116204948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47164905-T-C

116205050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47165009-C-T

116205517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47165473-A-G

http://identifiers.org/hco/5/GRCh38#116205948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47166099-C-A

116205948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47166099-C-T

116205951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47166102-C-T

116206129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47166256-T-A

116206129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47166256-T-C

116206261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47166360-G-T

116206312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47166404-A-G

116206759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47166546-A-G

116214679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47166900-A-G

116214797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47167003-C-T

116214829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47167035-G-C

116214923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47167119-C-G

116215018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47167218-C-T

116215946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47167996-C-T

116215968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47168018-A-G

http://identifiers.org/hco/5/GRCh38#116216142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47168190-C-A

http://identifiers.org/hco/5/GRCh38#116216214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47168288-A-C

116216454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47168610-T-G

116216481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47168639-C-T

http://identifiers.org/hco/5/GRCh38#116216517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47168675-A-C

116218423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47168981-G-A

116218570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47169126-A-G

116218595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47169164-G-C

116220182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47171244-C-T

116220336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47171385-G-T

116220372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47171418-A-G

116220592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47171618-T-G

116220599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47171624-C-G

116221788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47172181-T-C

116221882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47172275-T-C

116221899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47172292-A-G

116221995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47172374-T-C

116222095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47172476-G-A

116222095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47172476-G-T

116222333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47172702-C-G

116222333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47172702-C-T

116222450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47172774-A-G

116222466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47172790-T-G

116222539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47172844-C-T

116222679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47172963-A-G

116223654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -G-A

116223720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-T

116223800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-T

116223838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -T-G

http://identifiers.org/hco/5/GRCh38#116233546-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47183181-A-C

116233631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47183088-G-A

116233631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47183088-G-C

116233728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47183003-G-C

116233728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47183003-G-T

116233907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47182855-A-G

116234015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47182781-T-A

116234103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47182720-T-C

116234116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47182707-A-G

116234488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47182363-C-T

116234542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47182321-A-T

116234610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47182255-G-C

116234749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47182113-G-C

http://identifiers.org/hco/5/GRCh38#116234762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47182100-A-C

116234777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47182093-A-G

116234790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47182080-G-T

116234926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47181959-T-G

116235038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47181852-A-G

http://identifiers.org/hco/5/GRCh38#116235107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47181798-C-A

116235325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47181570-G-A

116235328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47181567-G-C

116235329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47181566-G-A

116235329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47181566-G-C

116237804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47179702-T-A

116237816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47179690-T-A

116237852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47179654-A-G

116238091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47179419-C-T

116238216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47179304-G-A

116238332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47179188-T-C

116238354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47179167-G-A

116238400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47179121-A-G

116238488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47179063-T-C

116238502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47179049-A-G

116238833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47178763-C-T

http://identifiers.org/hco/5/GRCh38#116238834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47178762-A-C

116238847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47178749-T-A

116238896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47178702-G-A

116238896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47178702-G-T

116239056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47178550-T-C

116239056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47178550-T-G

116239111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47178501-T-G

116258842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47187794-A-G

116259006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47187927-T-A

116259006-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47187927-T-G

http://identifiers.org/hco/5/GRCh38#116259102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47188121-A-C

116259102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47188121-A-T

116259156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47188164-G-A

116259156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47188164-G-T

116259554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47188660-T-G

116259575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47188678-A-G

http://identifiers.org/hco/5/GRCh38#116259763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47188854-A-C

116259763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47188854-A-G

116259787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47188874-C-T

116260215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47190110-T-C

116260368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47190263-A-G

http://identifiers.org/hco/5/GRCh38#116260531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47190435-C-A

116260931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47191222-A-G

116261048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47191318-C-T

116261415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47191664-C-G

116261545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47191777-G-A

116261671-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47191864-T-G

116261972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47193628-A-G

116262348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47193992-C-T

http://identifiers.org/hco/5/GRCh38#116262402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47194045-A-C

116262406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47194049-G-A

116262803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47196021-T-A

116262975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47196156-G-A

116264296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47196637-T-G

http://identifiers.org/hco/5/GRCh38#116264602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47196953-C-A

http://identifiers.org/hco/5/GRCh38#116264605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47196956-A-C

116265088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47197420-G-A

116265099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47197433-C-G

116265099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47197433-C-T

116265122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47197456-G-C

116265194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47197543-G-A

116265233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47197578-A-G

116273383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47198235-C-T

116273497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47198318-T-A

116273599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 47198420-C-T

116273995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47198798-A-G

116274019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47198824-A-G

116274186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47198974-A-G

116274600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47199361-A-G

116274667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47199434-C-T

116274729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47199486-C-T

116274758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47199518-T-G

116274870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47199604-T-G

116276652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47205215-G-A

116276772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47205312-T-A

116276772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47205312-T-C

116277085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47205589-G-A

http://identifiers.org/hco/5/GRCh38#116277127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47205625-C-A

116277136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47205634-A-G

116277149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47205647-C-T

116277153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47205651-C-G

116277653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47206107-G-A

116277653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47206107-G-C

116277776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47206302-G-A

http://identifiers.org/hco/5/GRCh38#116277781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47206307-C-A

http://identifiers.org/hco/5/GRCh38#116278022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47206565-A-C

116278039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47206582-T-A

116278104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47206640-C-G

116278114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47206653-T-G

116278170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47206703-A-G

116278216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47206734-T-C

http://identifiers.org/hco/5/GRCh38#116278422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47206914-C-A

116278711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47207183-A-G

116278756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47207231-C-T

116278843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47207312-G-A

116278935-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47207366-A-T

116278973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47207402-A-G

116278973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47207402-A-T

116278980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47207409-A-G

http://identifiers.org/hco/5/GRCh38#116279118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47207505-A-C

116279121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47207508-A-G

116279218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47207602-G-C

116279337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47207725-C-T

116279445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47207855-G-A

116279559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47207944-A-G

116279564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47207949-T-C

116279700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47208079-G-A

116279718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47208096-G-A

116279736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47208114-C-T

116280172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47208548-C-T

116280286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47208636-A-G

http://identifiers.org/hco/5/GRCh38#116280660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47208740-A-C

http://identifiers.org/hco/5/GRCh38#116280695-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47208770-A-C

116280709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47208783-C-G

116280816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47208892-T-C

116280878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47208956-C-G

116280879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47208957-T-C

116281042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47209085-T-A

116281343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47209361-T-C

116281352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47209370-T-C

116281362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47209380-A-G

116281386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47209404-A-G

http://identifiers.org/hco/5/GRCh38#116281443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47209447-A-C

116281443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47209447-A-G

116281480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47209466-G-A

116281480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47209466-G-T

116281492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47209478-A-G

116281567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47209549-G-A

http://identifiers.org/hco/5/GRCh38#116282104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47210011-C-A

116282104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47210011-C-T

116289815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47217773-C-T

116290134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47218090-G-A

116290415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47218301-T-C

http://identifiers.org/hco/5/GRCh38#116290547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47218430-A-C

116290655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47218567-C-G

116290655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47218567-C-T

116290829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47218704-G-C

http://identifiers.org/hco/5/GRCh38#116290901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47218764-A-C

116290901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47218764-A-G

116290902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47218765-T-C

116291066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47218920-G-T

116291138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47218992-T-C

116291288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47219138-G-A

116291292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 47219142-A-G

http://identifiers.org/hco/5/GRCh38#116291519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47219321-C-A

116291519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 47219321-C-T

116291520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 47219322-C-T

116291595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47219395-A-T

116291619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47219419-T-C

116291652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47219448-T-A

116291652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47219448-T-C

116291788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47219587-T-G

116291861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47219656-C-T

116292165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47219803-G-A

116292302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47219940-G-C

116292309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47219947-T-C

116292309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47219947-T-G

116292314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47219956-T-C

http://identifiers.org/hco/5/GRCh38#116292324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47219967-A-C

116292333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47219977-A-G

116292337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47219981-T-C

116292400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220041-A-G

116292400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220041-A-T

116292540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47220188-G-A

116292540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47220188-G-C

116292540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47220188-G-T

116292545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47220193-G-A

116292545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47220193-G-C

116292545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 47220193-G-T

116292588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220236-T-C

116292684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220331-T-G

116292690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220337-T-C

116292727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220367-T-A

116292727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220367-T-C

116292770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220460-G-A

116292770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220460-G-T

116292797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220585-G-T

116292811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220598-G-A

116292811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220598-G-T

116292822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220607-A-G

116292822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220607-A-T

116292824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220609-T-C

116292855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220640-A-G

116292856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220641-G-T

116292979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220752-G-A

http://identifiers.org/hco/5/GRCh38#116293011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47220783-A-C

116293017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220790-A-G

116293019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220792-G-A

116293019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220792-G-T

116293092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220864-T-C

116293092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220864-T-G

116293215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220973-G-A

116293220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220978-A-G

116293220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47220978-A-T

116293264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 47221030-C-T

116293327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47221092-T-A

116293349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47221114-T-C

116293475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47221189-A-T

116293572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47221284-T-G

116293622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47221336-A-G

116293622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47221336-A-T

116293673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47221375-A-G

http://identifiers.org/hco/5/GRCh38#116293757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47221469-C-A

116293757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47221469-C-G

116294559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47222490-C-T

116294607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47222538-C-G

116294607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47222538-C-T

116295194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47223143-G-A

116295940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47223997-C-G

116296290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47224341-G-T

116296551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47224602-G-T

116296638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47224688-G-C

http://identifiers.org/hco/5/GRCh38#116296687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47224737-C-A

116296695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47224745-A-G

116296752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47224803-C-T

116296986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47225045-A-G

http://identifiers.org/hco/5/GRCh38#116297238-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47225276-A-C

116297243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47225281-A-G

116297336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47225390-G-A

116297938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47226558-T-A

116297953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47226573-C-T

116297996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47226612-A-T

116298051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47226678-C-G

116298065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47226692-A-G

116298152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47226761-A-G

http://identifiers.org/hco/5/GRCh38#116298235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47226834-C-A

116298235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47226834-C-T

116298255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: non coding transcript exon variant
orthologous variants: 47226855-G-T

116298279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: non coding transcript exon variant
orthologous variants: 47226879-G-A

116298279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: non coding transcript exon variant
orthologous variants: 47226879-G-T

116298583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227134-C-G

116298583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227134-C-T

116298902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227438-G-A

116298968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227507-T-G

116298969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227508-G-T

116298970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227509-C-T

116299045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227579-G-A

116299205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227728-C-G

116299205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227728-C-T

116299613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228158-G-A

116299691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228237-G-C

116299920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228396-T-A

116300023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228493-G-A

116300041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228511-A-G

116300088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228557-G-T

116300114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228577-T-A

116300202-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228666-G-C

116300229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228686-C-T

http://identifiers.org/hco/5/GRCh38#116300947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47229446-A-C

116300947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47229446-A-G

116300947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47229446-A-T

116300983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47229478-T-G

116301037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47229528-T-C

116301207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47229676-T-G

116301279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47229746-A-G

http://identifiers.org/hco/5/GRCh38#116301482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47229922-A-C

116301598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230038-G-T

http://identifiers.org/hco/5/GRCh38#116301649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47230075-A-C

116301841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230268-A-G

116301889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230313-T-C

116301904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230328-G-A

116301909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230333-C-G

116302019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230451-A-G

116302155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230611-A-G

116302281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230714-A-G

http://identifiers.org/hco/5/GRCh38#116302355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47230782-C-A

116302377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47230804-T-G

116302461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230891-G-A

116302495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230925-T-C

116302615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47231048-C-T

116302713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47231178-A-G

116303084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47231533-A-G

116303451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47231858-T-C

http://identifiers.org/hco/5/GRCh38#116303460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47231870-C-A

116303460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47231870-C-T

116303470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47231880-G-C

116303509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47231919-C-G

116303509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47231919-C-T

116303582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47231993-C-T

116303782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232173-A-G

116303819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232211-G-A

116303819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232211-G-T

116303825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232217-G-A

116303825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232217-G-T

116303829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232221-G-A

116303829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232221-G-T

116303833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232225-G-A

116303833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232225-G-T

116303841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232233-G-A

116303843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232235-G-A

http://identifiers.org/hco/5/GRCh38#116303923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47232325-C-A

116303923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232325-C-T

116303930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232332-C-T

116303950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232352-G-T

116304044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47232434-G-A

116304044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47232434-G-T

http://identifiers.org/hco/5/GRCh38#116304051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47232446-C-A

116304051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47232446-C-T

http://identifiers.org/hco/5/GRCh38#116304052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47232447-A-C

116304083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47232470-A-G

116304121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47232509-C-T

116304150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232534-T-C

116304151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232535-G-A

116304165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232549-G-A

http://identifiers.org/hco/5/GRCh38#116304268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47232610-A-C

116304268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232610-A-T

116304384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232670-T-A

116304520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232809-C-T

116304831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233087-C-T

116304879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233122-C-T

116304961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233187-C-T

116304991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233213-T-A

116304991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233213-T-G

116306360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233299-T-G

116306376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233320-G-C

116306442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233373-A-G

116306458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233386-T-A

116306483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233411-C-T

116306564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233482-G-A

116306587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233503-T-C

http://identifiers.org/hco/5/GRCh38#116306606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47233531-A-C

116306607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233532-A-G

116306683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233585-C-T

http://identifiers.org/hco/5/GRCh38#116306699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47233605-C-A

116306699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233605-C-G

http://identifiers.org/hco/5/GRCh38#116306774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47233679-C-A

116306774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233679-C-G

116306796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47233730-T-C

116306820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47233767-G-A

116306840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47233787-G-A

116306840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47233787-G-C

116306949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233893-G-A

http://identifiers.org/hco/5/GRCh38#116307093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47234037-A-C

116307101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47234045-A-G

116307397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47234351-G-C

116307397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47234351-G-T

116307398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47234352-C-T

116307493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47234435-T-C

http://identifiers.org/hco/5/GRCh38#116307697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47234840-C-A

116308206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47235388-T-C

116308250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47235439-C-G

116308280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47235467-C-G

116308384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47235555-T-C

116308384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47235555-T-G

116308410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47235586-T-C

116308459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47235638-A-T

116313825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47254555-G-C

116313868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47254496-G-A

116313997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47254411-G-A

http://identifiers.org/hco/5/GRCh38#116314036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47254389-C-A

116314036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47254389-C-G

116314036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47254389-C-T

116314067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47254356-G-A

116314112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47254312-G-A

116314186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47253878-A-G

116314217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47253848-A-G

116315155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47253088-A-G

116315182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47253061-A-G

116315235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47252870-G-A

116315246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47252859-A-T

116315394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47252695-G-T

116315472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47252640-C-T

http://identifiers.org/hco/5/GRCh38#116315556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47252554-C-A

116315686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47252423-A-G

116316318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47251865-C-T

116316352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47251834-T-C

http://identifiers.org/hco/5/GRCh38#116316384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47251804-C-A

116316406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47251785-G-A

116320858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47258600-A-G

116321159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47258914-G-A

116321170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47258925-G-A

http://identifiers.org/hco/5/GRCh38#116321186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47258941-A-C

116321186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47258941-A-G

116321246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47258996-G-C

116321263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47259013-A-T

116321393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47259306-T-C

116321428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47259336-G-T

116321465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47259374-G-A

116321836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47259736-A-G

116322214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260131-T-C

116322235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260145-C-T

116322307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260212-A-G

116322532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260431-G-A

116322578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260476-T-G

116322594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260492-A-T

116322791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260673-G-C

116322810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47260692-G-A

116342752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47267473-C-T

116342839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47267555-A-G

116342874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47267590-T-G

116343032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47267737-C-T

116343147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47267815-T-C

http://identifiers.org/hco/5/GRCh38#116343160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47267828-C-A

116343160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47267828-C-T

116349105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47268916-A-G

116349309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269068-G-C

116349383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269150-G-A

116349720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269520-A-G

116349947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269766-G-C

116350044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269868-G-A

116350062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47269879-T-C

116352988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270436-G-C

116353040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270486-G-A

116353040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270486-G-T

116353180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270659-A-G

116353331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270860-G-C

116353331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270860-G-T

116353391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47270918-T-G

116353553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271085-T-C

116353558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271090-G-C

116353592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271124-G-A

http://identifiers.org/hco/5/GRCh38#116353612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47271146-A-C

116353612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271146-A-G

116353651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271185-C-G

116353651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271185-C-T

116353741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47271251-G-C

http://identifiers.org/hco/5/GRCh38#116354637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47276588-A-C

116354712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47276662-C-G

116354742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47276700-A-G

116354861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47276796-G-T

116356682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47277342-C-T

116358304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47281147-T-A

116358336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47281182-G-A

http://identifiers.org/hco/5/GRCh38#116358644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47281422-A-C

http://identifiers.org/hco/5/GRCh38#116358705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47281507-C-A

116358705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47281507-C-G

116358868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47281696-T-C

116359036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47281862-C-T

116359061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47281894-G-A

116359069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47281902-C-G

116359133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47281969-T-C

116359508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282282-T-C

116359508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282282-T-G

116359591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282366-G-A

116359591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282366-G-C

116359653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282412-C-G

http://identifiers.org/hco/5/GRCh38#116359910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47282674-C-A

116360301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283062-T-C

116360308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283067-C-T

116360425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283182-G-C

116360454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283211-C-T

116360455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283212-G-A

116360719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283445-G-A

116360789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283506-T-G

116360813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283529-G-C

116360845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283569-C-T

116360886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283616-A-G

116361140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284007-G-T

116361161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284025-G-A

116361161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284025-G-T

116361214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284066-G-C

116361229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284081-G-A

116361386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284233-C-T

116361469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284277-C-T

116361490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284289-C-T

116361701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284448-C-G

116361701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284448-C-T

116361881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47284618-C-G

116361912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284649-A-G

116361963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284712-T-G

116362024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284770-T-A

116362190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284928-A-T

116362604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285336-G-C

116362750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285452-G-A

116362784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285475-G-T

116362837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285524-G-C

116363025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285856-T-C

116363053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47285889-G-A

116363625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47286650-G-A

116363643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47286668-G-A

116363643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47286668-G-T

116363901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47286932-T-A

116363901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47286932-T-C

116364006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287001-G-A

116364044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287036-C-T

116364710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287601-T-A

116364871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287740-A-T

116364878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287747-G-T

116364916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287786-G-A

116364916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287786-G-T

116364999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287869-A-G

116365028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287899-T-C

116365117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47287987-C-T

116365203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288073-C-T

116365305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288210-A-G

116365305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288210-A-T

116365359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288258-C-T

116365427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288297-T-C

116365460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288330-A-T

116365609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288511-A-G

116365649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288551-T-A

116366000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288866-T-C

116366025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47288891-G-C

116366345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289224-A-T

116366413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289289-G-A

116366434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289310-G-A

116366434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289310-G-T

116366507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289396-T-C

116366547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289447-G-A

116366547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289447-G-C

116366569-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289469-A-T

116366631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289526-A-G

116366660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289563-A-G

116366679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289582-A-G

116366679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289582-A-T

116367073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289814-T-C

116367129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289839-G-A

116367169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289876-T-C

116367229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47289931-G-A

116367672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47290299-A-G

116367916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47290704-A-G

116368292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47291077-C-G

116368522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47291311-G-T

116368824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47291550-G-A

116368824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47291550-G-C

116369045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47291766-A-G

116369203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47291900-T-G

116369395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47292078-G-A

116369495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47292174-T-A

116369495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47292174-T-G

116369555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47292219-T-G

116369719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47292385-C-G

116369719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47292385-C-T

116369764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47292430-G-A

116369904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47292794-T-C

116369950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47292839-A-G

116369982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47292871-G-C

116370032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47292922-C-T

116370040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47292930-C-G

http://identifiers.org/hco/5/GRCh38#116370111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47293003-A-C

http://identifiers.org/hco/5/GRCh38#116370260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47293136-A-C

116370273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47293165-C-T

116370365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47293255-C-G

116370365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47293255-C-T

116370596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47293484-A-G

116370671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47293573-T-C

116370796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47293687-G-A

http://identifiers.org/hco/5/GRCh38#116371189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47294085-C-A

116371265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47294168-C-G

116371495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47294391-A-G

116371560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47294455-G-A

116371597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47294491-G-A

116371625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47294560-T-C

116371865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47294735-A-T

116371894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47294768-C-T

116371906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47294780-T-C

116372024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47294868-G-C

116372055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47294899-G-C

116372215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295180-A-T

116372233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47295212-G-C

116372299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295274-C-T

116372604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295599-A-G

116372675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295674-T-C

116372808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295794-C-G

116372894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47295852-T-C

116372978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 47295934-C-G

116372978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 47295934-C-T

116373052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47297185-G-C

116373057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47297190-G-C

116373057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47297190-G-T

116373155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47297276-C-T

116373167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47297288-T-C

116373191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47297312-C-T

http://identifiers.org/hco/5/GRCh38#116373459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47297571-A-C

http://identifiers.org/hco/5/GRCh38#116373524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47297633-C-A

116373575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47297677-G-A

116373628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47297733-A-G

116373723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47297827-C-T

116373786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47297872-C-T

116373841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47297922-T-C

116374499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47297978-G-A

116374561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47298031-C-G

116374577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47298047-G-A

116374577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47298047-G-T

116374660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47298133-C-T

116374771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47298248-C-G

116375171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47298629-C-G

116375171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47298629-C-T

116375342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47298797-C-T

116375463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47298887-G-A

116375671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47299094-A-T

116375812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47299236-C-T

116376038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47299414-G-A

116376096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47299472-G-A

116376315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47299685-G-A

116376392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47299756-G-C

116376490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47299853-C-G

116376490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47299853-C-T

116376507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47299870-A-G

116376996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47300739-A-G

116376996-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47300739-A-T

116377328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47301426-T-C

116377431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47302150-C-T

116377534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47302243-C-T

116377619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47302335-G-T

116377638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47302352-A-G

116377638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47302352-A-T

116377867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47302596-A-G

116378018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47302744-T-G

116378032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47302758-C-T

116378038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47302764-A-G

116378361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47303056-A-G

116378371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47303059-A-G

116378705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47303383-G-T

http://identifiers.org/hco/5/GRCh38#116379106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47303817-C-A

116379187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47303901-C-T

116379253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47303968-C-T

116379309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304020-C-T

http://identifiers.org/hco/5/GRCh38#116379361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47304072-A-C

116381633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304552-C-T

116381789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304718-G-C

116381900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304835-G-A

116381900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47304835-G-C

116382147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47305068-G-A

116382147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47305068-G-T

116382157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47305078-A-G

116382165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47305086-A-G

116382264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47305186-C-G

116382305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: non coding transcript exon variant
orthologous variants: 47305227-G-A

116382359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: non coding transcript exon variant
orthologous variants: 47305300-C-T

116382374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 47305315-G-T

116382379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 47305320-C-G

http://identifiers.org/hco/5/GRCh38#116382515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47305459-C-A

116382515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305459-C-G

116382515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305459-C-T

116382516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305460-G-A

116382516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305460-G-T

116382565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305511-A-T

116382719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47305668-T-G

116382869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47306288-C-T

116382872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47306291-G-A

116382959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47306374-G-T

116383010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47306431-G-A

http://identifiers.org/hco/5/GRCh38#116383153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47306573-A-C

116383158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47306578-A-G

http://identifiers.org/hco/5/GRCh38#116383313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47306820-C-A

116383313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47306820-C-G

116383313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47306820-C-T

116383659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47307109-A-G

116384506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47307587-A-T

http://identifiers.org/hco/5/GRCh38#116384581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47307637-A-C

116384826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47307921-G-A

116384833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47307933-A-G

116384979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308094-G-C

116384979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308094-G-T

116385605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308340-A-G

http://identifiers.org/hco/5/GRCh38#116385615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47308350-C-A

116385615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308350-C-T

116385779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47308522-G-A

http://identifiers.org/hco/5/GRCh38#116386056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47309731-A-C

116386077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47309785-A-G

116386103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47309831-T-G

116386303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47309982-C-T

116386498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47310143-C-T

116386672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47310322-G-A

116386763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47310422-A-G

116386835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47310495-A-G

116387028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47310686-C-T

116387046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47310704-C-T

116387126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47310785-G-C

http://identifiers.org/hco/5/GRCh38#116387149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47310806-C-A

116387149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47310806-C-T

116387219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47310867-T-C

http://identifiers.org/hco/5/GRCh38#116387391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47311015-A-C

116387393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311017-G-A

116387545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311111-C-T

116387549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311115-C-G

116387708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311272-G-A

http://identifiers.org/hco/5/GRCh38#116387765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47311326-A-C

116387795-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311356-A-T

116387847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311388-G-A

116388084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311623-T-C

116388315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311847-A-G

116388315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311847-A-T

116388342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47311870-A-T

116388574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47312855-A-G

116388640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47312924-G-A

116388657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47312939-C-T

116389025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47313297-C-T

116389127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47313387-G-A

116389254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47313513-A-G

116389339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47313598-T-G

116389361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47313620-T-C

116389442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47313720-G-A

116389872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47313809-A-G

116389941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47313878-T-C

116392864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47315133-G-C

116393083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47315360-T-A

116393135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47315403-G-T

116393144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47315411-G-C

http://identifiers.org/hco/5/GRCh38#116393176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47324047-A-C

116393222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47324082-A-G

116393373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47324323-A-G

116393848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47324908-G-T

116393999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47325040-T-A

116393999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47325040-T-C

http://identifiers.org/hco/5/GRCh38#116394530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47325681-C-A

116394605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47325741-T-C

116394605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47325741-T-G

116394615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47325751-G-A

116394894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47325982-T-A

116395100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47326186-G-T

116395113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47326199-A-G

116395165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327175-C-T

116395317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327314-G-C

116395339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327336-G-A

116395387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327382-G-A

116395387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327382-G-T

http://identifiers.org/hco/5/GRCh38#116395405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47327400-C-A

116395665-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327695-C-G

116395720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327749-C-T

116395751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327781-T-A

116395751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327781-T-C

116395854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327882-G-A

116395929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47327960-C-T

116395981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328012-A-G

116396044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328071-G-A

116396063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328090-G-A

116396063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328090-G-C

116396193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328212-G-C

116396193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328212-G-T

116396208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328227-G-A

116396209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328228-G-A

116396238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328261-A-G

116396426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328447-C-T

116396570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328578-G-T

116396575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328584-T-C

116396682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328659-G-T

116396742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328718-T-G

http://identifiers.org/hco/5/GRCh38#116396821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47328779-C-A

116396821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47328779-C-G

http://identifiers.org/hco/5/GRCh38#116397125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47329019-A-C

116397322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47329131-A-G

116397362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47329171-C-T

116397443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47329207-A-G

http://identifiers.org/hco/5/GRCh38#116397727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47329633-A-C

116397818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47329743-T-G

116397851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47329784-A-G

116398207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47330478-T-C

116398256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47330527-C-T

116398351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47330593-C-T

116398720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47330957-C-G

116398720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47330957-C-T

116398780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331017-T-C

116398780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331017-T-G

116398842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331082-T-A

116399089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331325-A-G

116399090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331326-T-C

116399100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331333-G-A

116399131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331364-C-T

116399160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331393-T-A

116399217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331452-C-G

116399217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331452-C-T

116399241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331533-T-G

116399291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331596-C-G

116399292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331597-C-T

116399293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331598-A-G

116399342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331656-G-A

116399342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331656-G-T

116399408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331705-G-A

http://identifiers.org/hco/5/GRCh38#116399487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47331773-C-A

116399487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: non coding transcript exon variant
orthologous variants: 47331773-C-T

116399593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: non coding transcript exon variant
orthologous variants: 47331869-T-C

116399684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331922-T-A

116399684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331922-T-C

http://identifiers.org/hco/5/GRCh38#116399688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47331926-C-A

116399688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331926-C-G

116399688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331926-C-T

116399694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331932-G-A

116399694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331932-G-T

116399757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47331991-C-T

116399865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332108-A-G

116400245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332693-G-A

116400391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47332838-A-G

116400587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333034-G-A

116400661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333106-C-T

116400732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333176-A-G

116400732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333176-A-T

116400859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333299-G-C

116400860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333300-A-G

116401414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333796-G-T

116401446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333816-A-G

116401457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47333827-A-G

116401679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334040-G-A

116401754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334116-G-A

116401813-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334187-T-G

116401820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334194-T-G

116401971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334330-G-T

116402021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334380-T-G

116402041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334400-G-A

116402310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334666-G-T

116402372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47334728-G-A

http://identifiers.org/hco/5/GRCh38#116402413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47334769-C-A

116402828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47335079-G-A

http://identifiers.org/hco/5/GRCh38#116402932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47335178-C-A

116403039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47335285-C-T

116403042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47335288-C-T

116403202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47335404-G-A

116403247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47335437-G-C

116403466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47335639-T-C

116403872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47335960-T-C

116403918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47336006-G-A

116404171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47336256-T-G

116404188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47336273-C-T

116404206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47336291-A-G

116404401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47336468-C-T

116404404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47336471-T-G

116404456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47336523-C-T

116404458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47336525-C-T

116404930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337153-G-C

116404930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337153-G-T

116404993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337273-A-G

116405079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337348-T-C

116405080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337349-T-C

116405087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337356-T-C

116405391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47337648-C-T

116406126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47338511-T-G

116406599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47339337-G-A

116406599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47339337-G-C

116406602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47339340-A-G

116406818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47339542-C-T

116406945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47339661-A-G

116407017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47339731-G-A

116407199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47339914-C-T

116407560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340274-G-A

http://identifiers.org/hco/5/GRCh38#116407925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47340624-C-A

116407925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340624-C-G

116407925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340624-C-T

116408051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340750-C-T

116408121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47340821-T-C

116408395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47341219-C-T

116408663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47341714-C-T

116408762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47341810-C-T

116409604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47342544-T-A

116410050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47342983-C-T

116410220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47343153-T-C

116410574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47343497-G-A

116410950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344078-T-A

116410950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344078-T-C

116410971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344099-T-A

116410971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344099-T-C

116411312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344442-G-C

116411450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344570-G-A

http://identifiers.org/hco/5/GRCh38#116411464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#47344582-C-A

116412214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344927-C-G

116412214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344927-C-T

116412227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344940-G-A

116412257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344970-A-G

116412287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47344999-C-T

116412416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30201
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47345125-A-G