http://identifiers.org/hco/13/GRCh38#91347727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115278442-C-A

91347727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: non coding transcript exon variant
orthologous variants: 115278442-C-T

http://identifiers.org/hco/13/GRCh38#91347855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115278567-C-A

91347855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: non coding transcript exon variant
orthologous variants: 115278567-C-T

91348024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115278695-C-T

91348033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115278704-G-A

91348033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115278704-G-C

http://identifiers.org/hco/13/GRCh38#91348124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#115278771-C-A

91348328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115278893-G-C

91348337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 115278904-G-C

91348671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115279242-G-A

91348673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115279244-A-G

91348755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115279322-C-G

91348986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115279558-G-C

91349026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115279601-T-G

91349132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115279722-C-T

91349219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115279809-A-G

91349227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115279816-G-T

91349358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115279953-G-A

91349366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115279961-A-G

91349402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115279990-G-T

91349410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115279998-A-G

91349434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115280022-G-T

91349475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115280067-C-T

91349574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115280186-C-T

91349790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115280413-C-T

http://identifiers.org/hco/13/GRCh38#91349948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115280547-A-C

91349948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115280547-A-G

http://identifiers.org/hco/13/GRCh38#91350110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#115280664-C-A

91350110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115280664-C-G

91350110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115280664-C-T

http://identifiers.org/hco/13/GRCh38#91350340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115280847-C-A

http://identifiers.org/hco/13/GRCh38#91350341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115280848-C-A

91350343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115280850-T-C

91350385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115280885-A-G

http://identifiers.org/hco/13/GRCh38#91350392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115280887-C-A

91350392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115280887-C-T

91350414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115280920-G-C

91350441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115280946-A-G

91350464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115280958-A-T

91350487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115280981-T-G

91350493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115280988-G-A

91350597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115281095-T-G

91350718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115281261-A-G

91351127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115281670-A-G

91351549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115282149-G-A

91351549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115282149-G-T

91352740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115282868-C-G

91352740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115282868-C-T

91353313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115283101-C-T

91353828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115283466-C-T

91353861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115283491-G-T

91353889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115283500-T-C

91353996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115283613-C-G

http://identifiers.org/hco/13/GRCh38#91354015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115283632-C-A

91354015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115283632-C-T

91354017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115283634-A-G

91354037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115283653-G-C

91354110-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115283722-T-A

http://identifiers.org/hco/13/GRCh38#91354130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115283743-C-A

91354130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115283743-C-T

http://identifiers.org/hco/13/GRCh38#91354202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115283784-C-A

91354210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115283792-C-T

91354267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115283865-A-G

91354302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115283904-C-T

91354332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115283932-T-C

91354639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115284209-A-T

91359868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115287709-C-T

91359877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115287721-G-A

91359877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115287721-G-C

91359884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115287728-T-C

91360134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115288084-G-A

91360202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115288140-T-A

91360202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115288140-T-C

91360704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115288624-G-A

91360941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115288950-A-G

91360949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115288958-G-T

91361196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115289319-T-G

91361441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115289531-C-T

91361588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115289686-T-C

91361633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115289736-A-G

91361840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115289945-A-T

91361882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115289985-A-G

91362123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 115290228-T-C

91362268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115290374-T-C

91362363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115290496-A-G

91363418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115291502-A-G

91363731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115291773-T-C

http://identifiers.org/hco/13/GRCh38#91370226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115300323-C-A

91370328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115300420-T-C

91370429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115300507-C-T

91370889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115300982-C-T

91371121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115301222-G-T

91371182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115301288-T-G

91371322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115301416-T-C

http://identifiers.org/hco/13/GRCh38#91371459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115301544-A-C

91371722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115301912-A-T

91371867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115302167-C-G

91371877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115302176-A-G

91379871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115303407-C-T

91379906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115303442-C-T

91379959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115303489-C-T

91379973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115303503-T-G

91380477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307075-G-C

http://identifiers.org/hco/13/GRCh38#91380521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115307118-C-A

91380561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307175-G-T

91380574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307188-C-T

91380675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307285-T-C

91380821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307427-C-T

91380833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307439-A-G

91380857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307463-A-G

91380888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307498-C-G

91380891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307501-G-A

91380891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307501-G-T

91381048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307650-C-G

91381138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307720-A-G

91381140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307722-G-A

91381268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115307839-A-G

91381461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308037-T-C

91381475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308051-T-C

http://identifiers.org/hco/13/GRCh38#91381519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115308093-A-C

91381519-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308093-A-T

91381670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308236-A-T

http://identifiers.org/hco/13/GRCh38#91381799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115308359-C-A

91381837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308401-T-C

http://identifiers.org/hco/13/GRCh38#91381844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115308408-A-C

91381869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308427-T-A

91381886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308448-A-G

91381901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308465-C-T

91382034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308623-C-T

91382066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308656-C-T

91382198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308779-T-A

91382277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308838-A-G

91382282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308843-C-T

91382328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115308883-T-C

91382476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115309029-G-C

91382567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115309120-C-T

http://identifiers.org/hco/13/GRCh38#91382894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115309644-C-A

91383118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115309944-G-A

91383118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115309944-G-T

91383128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115309953-C-T

91383147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115309960-T-A

91383164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115309976-G-A

91383310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115310125-G-A

91383367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115310838-T-C

91383453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115310923-T-C

91383500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115310959-A-G

91383528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115310987-G-A

91383732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115311199-A-G

91383871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115311336-G-A

91383871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115311336-G-T

91384336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115312495-G-A

91384337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115312497-G-T

91384341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115312501-T-G

91384347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115312506-C-T

91384579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115312733-A-G

91385025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115313271-C-G

91385031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115313277-A-G

91385108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115313339-G-C

http://identifiers.org/hco/13/GRCh38#91385720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115314002-A-C

91385995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115314272-A-G

91386200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115314445-A-G

91386403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115314627-T-C

91386421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115314645-A-T

91386530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115314825-T-G

http://identifiers.org/hco/13/GRCh38#91386570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115314870-C-A

91386570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115314870-C-T

91386588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115314888-G-C

91386588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115314888-G-T

91386660-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115314953-A-T

91386726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315008-G-C

91386733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315019-T-G

91386899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315168-A-T

91386957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315226-A-G

91387078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315339-G-A

91387078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315339-G-T

91387181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315441-T-C

91387181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315441-T-G

91387233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315485-A-G

http://identifiers.org/hco/13/GRCh38#91387288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115315539-A-C

91387288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315539-A-G

91387336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315549-A-G

91387336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315549-A-T

91387572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315711-C-T

91387587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315726-C-T

91387830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115315967-A-G

91388606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115316335-C-T

91388916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115316635-A-G

91389301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115317783-A-G

91389383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115317854-T-C

91389420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115317898-G-A

91389632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115318214-A-G

91389783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115318357-G-T

91389790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115318364-A-G

91390040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115318440-G-A

91390157-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115318557-T-A

91390157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115318557-T-C

91390265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115318665-G-A

91390286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115318686-T-C

91391078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115319012-G-C

91391091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115319025-G-A

91391150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115319083-G-A

91391150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115319083-G-T

91391239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115319164-G-A

91391253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115319177-G-A

91391610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115319500-C-T

http://identifiers.org/hco/13/GRCh38#91391866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115319754-A-C

91391998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115319901-C-T

91392014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115319917-A-G

91392063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115319970-A-G

91392641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115320683-T-C

91392672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115320715-T-C

91392749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115320882-A-G

91392776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115320902-G-A

91392805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115320932-G-A

91392805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115320932-G-C

91392819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115320952-C-G

http://identifiers.org/hco/13/GRCh38#91392834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115320969-A-C

91393212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115321328-C-T

91394995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115325901-G-A

91395041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115325954-G-T

91395106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115325999-C-T

http://identifiers.org/hco/13/GRCh38#91395314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#115326203-C-A

91395314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115326203-C-G

91395562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115326606-G-A

91395562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115326606-G-T

91395967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115327141-A-G

91396056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115327221-T-C

91396124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115327288-G-C

91396254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115327418-T-C

91396374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115327539-T-G

91396438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115327594-T-G

91396584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115327746-T-C

91396589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115327751-C-T

91396747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115327882-A-G

91396795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115327925-G-A

91396825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115327954-A-G

91396830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115327959-A-G

91396919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115328044-T-C

91396919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115328044-T-G

91396954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 115328072-A-G

91397129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: non coding transcript exon variant
orthologous variants: 115328213-A-G

91397142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: non coding transcript exon variant
orthologous variants: 115328226-T-C

91397238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 115328316-T-G

91397363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: non coding transcript exon variant
orthologous variants: 115328437-A-G

91397433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23564
most severe consequence: non coding transcript exon variant
orthologous variants: 115328561-T-C