91692425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4364570-A-G

91692439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4364556-T-G

91692445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4364550-G-T

91692567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4363792-A-G

91692948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4363253-G-A

http://identifiers.org/hco/7/GRCh38#91693220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4362977-C-A

91693323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4362880-C-T

91693352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4362851-G-T

91693378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4362830-G-A

91693378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4362830-G-T

91693388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4362820-A-G

91693422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: non coding transcript exon variant
orthologous variants: 4362782-A-G

91693505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4362696-A-T

91693586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4362617-A-G

91693586-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4362617-A-T

91693693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4362509-A-G

91693976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4362283-G-A

91693976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4362283-G-T

91694243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4361993-T-A

91694243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4361993-T-C

91694265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4361968-G-A

91694265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4361968-G-C

91694587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4361642-T-G

91694660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4361571-A-G

91694864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4361374-G-C

91695466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4360852-T-C

91695566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4360764-T-C

91695627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4360686-C-G

91695629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4360684-G-A

91696195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4358574-G-C

91696447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4358060-A-G

91696455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4358052-C-T

91696672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4357858-T-G

91696722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4357820-G-A

91696733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4357809-T-G

91696881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4357674-C-G

http://identifiers.org/hco/7/GRCh38#91696913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4357642-C-A

91696965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4357589-C-T

91697129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4357445-C-G

91697184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4357269-A-G

91697509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4356778-A-G

91697617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4356677-T-C

http://identifiers.org/hco/7/GRCh38#91697838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4356571-C-A

91717572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4354418-C-T

91717677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4354319-G-C

91717823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4354177-G-A

91718117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4353854-T-A

91718151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4353820-G-A

91718374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4353597-T-C

http://identifiers.org/hco/7/GRCh38#91718622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4353364-C-A

91718636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4353350-T-C

91718858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4353132-A-G

91718873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4353117-T-C

http://identifiers.org/hco/7/GRCh38#91719480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4351304-C-A

91719480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4351304-C-T

91719507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4351276-A-G

91719533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4351250-G-A

91729708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4343198-C-T

91729954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4342974-G-A

http://identifiers.org/hco/7/GRCh38#91730092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4342838-A-C

91730336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4342598-A-G

91730387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4342541-T-C

91730528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4342415-T-C

91731151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4342095-A-T

91731434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4341868-C-G

91731777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4340327-A-G

91731808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4340278-G-A

91731946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4340141-T-C

91731999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4340087-T-C

91732032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4340055-T-C

http://identifiers.org/hco/7/GRCh38#91732109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4339978-A-C

91732137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4339952-G-T

91732397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4339697-T-C

91732397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4339697-T-G

91743599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4339060-T-C

http://identifiers.org/hco/7/GRCh38#91744179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4338150-A-C

91744209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4338124-G-C

91744483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4337879-A-G

91769553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4325956-T-C

91769633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4325898-A-T

91769797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4325737-T-C

http://identifiers.org/hco/7/GRCh38#91770301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4325537-C-A

91770477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4325382-A-G

91770576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4325284-G-A

91770978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4324901-G-A

91770981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4324898-G-C

http://identifiers.org/hco/7/GRCh38#91771193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4324727-C-A

91771687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4324263-A-G

91771707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4324242-C-G

91771893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4324055-C-T

91772073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4323884-G-T

91772074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4323883-A-G

http://identifiers.org/hco/7/GRCh38#91772273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4323495-A-C

91772273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4323495-A-G

91772273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4323495-A-T

http://identifiers.org/hco/7/GRCh38#91772317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4323452-C-A

91772390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4323378-C-G

91772848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4322950-T-C

91773697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4322166-T-C

91773782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4322084-G-A

91773832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4322030-T-C

91774023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4321851-G-C

91774122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4321754-G-A

91774159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4321718-A-G

91774280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4321608-G-T

91774305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4321583-T-C

91774323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4321565-T-C

http://identifiers.org/hco/7/GRCh38#91774493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4321405-A-C

91774508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4321390-C-T

91774538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4321362-A-G

91776728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4320993-T-C

91776872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4320856-G-T

91777024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4320698-G-A

91777346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4320396-G-A

91777346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4320396-G-T

91777459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4320285-C-T

91777497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4320235-A-G

http://identifiers.org/hco/7/GRCh38#91777504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4320228-C-A

91777569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4320187-C-T

http://identifiers.org/hco/7/GRCh38#91777728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4320026-A-C

91777882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4319882-A-T

91778317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4319468-T-G

91778327-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4319458-G-C

91778327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4319458-G-T

91778400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4319372-C-T

http://identifiers.org/hco/7/GRCh38#91778405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4319367-A-C

91778477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4319298-T-C

91779791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4318793-A-G

91779881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4318634-T-C

91779927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4318588-C-T

http://identifiers.org/hco/7/GRCh38#91780200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4318331-A-C

91780510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4318063-T-C

http://identifiers.org/hco/7/GRCh38#91780683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4317894-A-C

91780784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4317794-A-G

http://identifiers.org/hco/7/GRCh38#91780880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4317700-A-C

91780963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4317626-A-G

91780980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4317613-G-A

91781020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4317573-G-A

http://identifiers.org/hco/7/GRCh38#91781109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4317264-C-A

91781231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4317158-T-G

91781234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4317155-G-C

91781261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4317123-C-T

91781265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4317119-G-A

http://identifiers.org/hco/7/GRCh38#91781554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4316856-A-C

http://identifiers.org/hco/7/GRCh38#91781594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4316817-A-C

91781689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4316747-T-C

91781744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4316694-A-G

91781764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4316674-T-C

91781966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4316481-A-G

91782229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4316422-C-T

91782435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4316205-A-G

91782453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4316137-T-C

91782491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4316103-G-A

91782547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4316055-C-T

91782671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4315942-T-C

91782679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4315939-T-G

91782797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4315914-G-A

91782918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4315795-G-A

91782918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4315795-G-T

91783099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4315641-A-G

91783315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4315381-C-T

91783331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4315282-G-T

91783489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4315142-G-A

91783697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4314928-T-A

91783967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4314656-G-A

91783967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4314656-G-C

91784528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4314096-T-C

91784840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4313799-C-G

http://identifiers.org/hco/7/GRCh38#91785073-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4313093-A-C

http://identifiers.org/hco/7/GRCh38#91785347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4312608-A-C

91785982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4311855-A-G

91785990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4311847-G-A

91785990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4311847-G-T

http://identifiers.org/hco/7/GRCh38#91786048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4311783-A-C

91786048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4311783-A-G

91786165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4311677-G-C

91786893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4310776-C-T

91786915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4310754-C-T

91787075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4310576-T-C

http://identifiers.org/hco/7/GRCh38#91787101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4310551-A-C

91787101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4310551-A-G

91787120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4310531-A-G

91787310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4310359-T-G

91787504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4310075-T-C

http://identifiers.org/hco/7/GRCh38#91787919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4309708-C-A

91787919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4309708-C-T

91787995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4309207-T-C

91788011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4309191-A-G

91788079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4309121-G-C

91788393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4308387-A-T

91788447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4308344-A-G

91788558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4308237-A-T

91788902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4307939-A-G

91788996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4307847-G-A

91789023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4307820-C-T

91789197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4307631-T-C

91789296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4307529-T-C

91789396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4307428-T-C

91789467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4307358-T-C

91789795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4307033-A-G

91789855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4306974-A-T

91790059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4306765-C-T

91790060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4306764-G-A

91790110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4306722-A-G

91790152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4306679-G-C

91796449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4304371-A-G

91796452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4304368-G-T

91796489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4304330-A-G

http://identifiers.org/hco/7/GRCh38#91796556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4304263-C-A

91796650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4304173-A-G

91796685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4304138-A-G

91797006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4303879-T-C

http://identifiers.org/hco/7/GRCh38#91797008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4303877-C-A

91797008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4303877-C-T

91797902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4303141-G-A

91798048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4302998-G-A

91798049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4302997-T-C

91798248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4302829-G-A

91798248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4302829-G-T

91798270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4302806-A-G

91798382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4302700-C-T

91798524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4299837-A-T

91799282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4299150-A-G

91799468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4298978-C-T

91799698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4298746-C-T

http://identifiers.org/hco/7/GRCh38#91809335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4296306-C-A

91809428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4296217-C-T

http://identifiers.org/hco/7/GRCh38#91809592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4296074-C-A

91809753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4295913-C-T

91809777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4295888-T-C

91809852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4295810-G-T

91810120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4295599-T-C

91810120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4295599-T-G

91811142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4295260-T-C

91811201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4295212-T-C

http://identifiers.org/hco/7/GRCh38#91811583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4294839-C-A

91811584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4294838-T-A

91811609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4294813-C-T

91811706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4294724-G-C

91812000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4294433-T-C

91812071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4294366-A-G

91812072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4294365-T-C

91812239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4294210-A-G

http://identifiers.org/hco/7/GRCh38#91812431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4294011-C-A

91812431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4294011-C-G

91812502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4293940-C-T

91812869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4292889-A-T

91813607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4291864-G-A

91813654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4291825-C-G

91817534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4291238-C-T

91817728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4291051-A-G

91817758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4290617-T-C

91817909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4290476-G-A

91817918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4290467-T-C

91818154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4290249-C-T

91818427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4290122-G-C

91818888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4289155-T-C

91826233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4288050-G-A

91826668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4287618-A-G

http://identifiers.org/hco/7/GRCh38#91826737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4287558-C-A

91826737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4287558-C-G

http://identifiers.org/hco/7/GRCh38#91827024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4287297-C-A

91827137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4287180-C-G

91827212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4287148-G-A

91827225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4287135-T-C

91827577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4286720-G-A

91827577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4286720-G-T

91827643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4286654-A-G

91828510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4286262-T-C

91828582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4285807-C-T

91828697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4285693-G-A

91828739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4285611-G-A

91829159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4285228-G-A

91829257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4285137-T-A

91829636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4284777-C-G

91829760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4284655-T-G

http://identifiers.org/hco/7/GRCh38#91830325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4284415-A-C

91830777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4283226-G-T

91830891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4283101-C-T

91832684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4282726-T-G

91833210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4280955-C-T

91833437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4280742-T-C

91833458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4280721-C-T

http://identifiers.org/hco/7/GRCh38#91833825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4280553-C-A

91833882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4280502-T-G

91834363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4280044-G-A

91834363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4280044-G-C

91834918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4279662-T-C

91834963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4279616-C-G

91835465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4279106-G-A

91835507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4279055-C-T

91835930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4278645-G-C

91836075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4278521-C-T

91837173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4277526-G-A

91837173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4277526-G-C

91837282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4277053-G-T

91837927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4276465-T-G

91838228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4276176-T-C

91838232-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4276172-T-A

http://identifiers.org/hco/7/GRCh38#91838331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4276100-A-C

91838929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4275521-T-C

91839218-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4275256-C-G

91839226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4275248-C-T

http://identifiers.org/hco/7/GRCh38#91839363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4275120-C-A

91839423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4275070-T-A

91841332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4274631-T-A

91841596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4274457-C-T

91841674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4274381-C-T

91841788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4274266-A-G

91841972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4274078-A-G

91845477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4272966-T-G

91845693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4272834-A-G

91845886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4272650-C-T

91846483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4272435-T-C

91846493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4272425-G-T

91846529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4272390-A-G

91847098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4271841-T-C

91847112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4271826-G-C

91847112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4271826-G-T

91847193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4271741-T-C

91847482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4271474-T-G

91847526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4271431-A-G

91847614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4271343-T-C

91847646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4271311-T-C

91848042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4270928-C-T

91848102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4270866-A-G

91848232-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4270742-G-C

91848319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4270651-T-C

91848445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4270540-T-C

91848481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4270326-A-G

91848558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4270116-A-G

91848735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4269945-G-A

91849174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4269483-T-A

91849390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4269312-A-G

91849662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4269068-C-T

91865396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4260143-C-T

91865537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4260006-A-G

91865785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4259442-G-T

http://identifiers.org/hco/7/GRCh38#91866062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4259147-C-A

91866483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4252296-T-C

91866614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4252170-T-A

91867082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4251222-C-T

91867228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4251043-G-A

91867288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4250978-A-G

91867498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4250809-G-C

91867498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4250809-G-T

91867638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4249346-C-T

91867665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4249321-G-A

91867665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4249321-G-T

91867666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4249320-C-T

91867717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4249249-C-T

91871157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4248985-A-G

91873774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 4247330-A-G

91873774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 4247330-A-T

http://identifiers.org/hco/7/GRCh38#91873811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4247293-A-C

91873817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 4247287-T-C

91873880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 4247224-C-T

91873989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 4247115-C-G

http://identifiers.org/hco/7/GRCh38#91873990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4247114-C-A

91873990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 4247114-C-T

http://identifiers.org/hco/7/GRCh38#91874060-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/5/GRCm39#4247044-A-C

91874394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 4246710-G-A

http://identifiers.org/hco/7/GRCh38#91874462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4246642-A-C

91874613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 4246485-T-G

91874623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 4246475-A-G

91874650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 4246448-G-A

91874677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 4246421-A-G

91874799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4246298-G-A

91874799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4246298-G-C

91874799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4246298-G-T

91874801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4246296-A-T

91874826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4246275-A-G

91874828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4246273-T-C

http://identifiers.org/hco/7/GRCh38#91875695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4245869-C-A

91875695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4245869-C-G

91876933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 4244351-G-C

http://identifiers.org/hco/7/GRCh38#91877035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4244251-A-C

91877062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4244224-A-G

91877382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4243945-T-A

91879870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4243195-A-G

91879890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4243175-T-A

91879907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4243156-G-T

91879953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4243086-T-C

91879974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4243065-T-C

91880042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4242983-A-G

91880143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4242885-G-A

91880143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4242885-G-T

91880152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4242877-T-C

http://identifiers.org/hco/7/GRCh38#91880200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#4242846-C-A

http://identifiers.org/hco/7/GRCh38#91880208-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4242838-A-C

http://identifiers.org/hco/7/GRCh38#91880227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4242821-C-A

91880227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4242821-C-G

91880227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4242821-C-T

91880256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4242790-A-G

91880256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4242790-A-T

91880421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4242634-G-T

91880427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4242628-G-C

91880427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4242628-G-T

91880460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4242610-G-T

91880488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4242588-G-A

91880488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4242588-G-T

91880515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 4242565-A-G

http://identifiers.org/hco/7/GRCh38#91880519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4242561-C-A

91880567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4242527-T-G

91880636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 4242463-T-C

91880660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4242437-G-A

91880660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 4242437-G-T

http://identifiers.org/hco/7/GRCh38#91880673-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#4242410-C-A

91880673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21463
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 4242410-C-T