http://identifiers.org/hco/13/GRCh38#105702812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7878059-C-A

105703799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7878638-A-G

http://identifiers.org/hco/13/GRCh38#105704196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7879020-C-A

105704481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7879299-G-T

105704506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7879325-C-T

http://identifiers.org/hco/13/GRCh38#105705591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7881101-C-A

105705734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7881134-A-G

105705824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7881229-A-G

105705943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7881335-G-A

http://identifiers.org/hco/13/GRCh38#105706143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7881497-C-A

105706177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7881521-G-A

http://identifiers.org/hco/13/GRCh38#105706277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7881620-A-C

105706353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7881697-A-G

105706596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 7881933-G-T

105706604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7881941-A-G

105706751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7882077-G-T

http://identifiers.org/hco/13/GRCh38#105706796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7882120-C-A

105706796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7882120-C-T

105706870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7882163-G-T

105706910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7882216-C-T

105707023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7882306-T-C

105707236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: non coding transcript exon variant
orthologous variants: 7882521-T-C

105707237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: non coding transcript exon variant
orthologous variants: 7882522-C-T

105707413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: non coding transcript exon variant
orthologous variants: 7882689-T-C

105707610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: non coding transcript exon variant
orthologous variants: 7882871-G-T

105707628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 7882892-A-G

105707666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7882929-C-T

105707920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7883195-A-G

105707921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7883196-A-T

http://identifiers.org/hco/13/GRCh38#105707941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7883215-C-A

105707941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7883215-C-T

105708063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7883336-G-A

105708584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7885823-T-A

105708588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7885827-T-C

105708733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7885969-G-A

105708855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7886058-T-C

http://identifiers.org/hco/13/GRCh38#105718347-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7891884-A-C

105718669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7892203-G-T

105718812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7892352-G-T

105718883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7892424-G-A

105718990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7892523-C-T

105719059-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7892582-A-T

105719411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7893305-A-G

105719413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7893307-A-G

105719483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7893386-A-G

105719555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7893443-T-C

105719577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7893457-G-T

105719584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7893466-A-G

105719797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7893650-A-G

105719820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7893675-G-A

105719980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7893840-G-A

105720189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7894052-G-A

105720259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7894121-A-G

105720339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7894184-A-G

105720339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7894184-A-T

http://identifiers.org/hco/13/GRCh38#105720551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7894388-C-A

105720551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7894388-C-T

105720927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7894725-G-A

105720927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7894725-G-C

105721413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7895335-T-A

105721603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7895516-A-G

105721603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7895516-A-T

105721637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7895550-G-A

105721744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7895650-C-T

105721755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7895672-G-A

105721948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7895887-T-A

105721985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7895921-C-T

105722060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7895997-T-C

105722451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7896368-A-G

105722507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7896422-T-C

105722624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7896548-T-C

105722681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7896605-G-A

http://identifiers.org/hco/13/GRCh38#105722696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7896618-C-A

105722733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7896650-T-A

105722775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7896689-G-A

105723554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7899690-A-G

105723742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7899884-A-G

http://identifiers.org/hco/13/GRCh38#105724084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7900204-C-A

105724084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7900204-C-T

105724099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7900219-T-C

105724288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7900387-T-A

105724305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7900399-A-T

105724344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7900423-T-C

105724365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7900442-G-A

http://identifiers.org/hco/13/GRCh38#105724380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7900457-C-A

105724380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7900457-C-T

105724407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7900484-A-G

105724407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7900484-A-T

105726618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7902350-C-T

http://identifiers.org/hco/13/GRCh38#105726634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7902366-C-A

105726634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7902366-C-G

105726634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7902366-C-T

105726644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7902376-T-C

http://identifiers.org/hco/13/GRCh38#105726677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7902409-A-C

105726677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7902409-A-G

http://identifiers.org/hco/13/GRCh38#105726718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7902451-C-A

105726718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7902451-C-G

105726718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7902451-C-T

105726746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7902469-T-C

105726856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7902554-C-T

105727061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7902761-T-C

http://identifiers.org/hco/13/GRCh38#105727105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7902805-A-C

105728168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7903759-C-G

105728405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7903998-A-T

105728661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7904250-C-T

105728958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7904545-T-C

105729045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7904622-G-A

105729387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905372-A-G

105729469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905445-C-T

http://identifiers.org/hco/13/GRCh38#105729645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7905627-C-A

http://identifiers.org/hco/13/GRCh38#105729696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7905660-C-A

105729878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905840-T-A

105729878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905840-T-C

105729878-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905840-T-G

http://identifiers.org/hco/13/GRCh38#105729880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7905842-C-A

105729880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905842-C-G

105729880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905842-C-T

105729954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905923-G-T

105729962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905931-T-C

105729973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905942-G-A

105729973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905942-G-T

105729995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905964-G-A

105730008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905976-A-G

105730009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7905977-G-T

http://identifiers.org/hco/13/GRCh38#105730067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7906035-C-A

105730067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7906035-C-T

http://identifiers.org/hco/13/GRCh38#105730075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7906040-C-A

http://identifiers.org/hco/13/GRCh38#105730098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7906063-C-A

105730098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7906063-C-T

105730174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7906117-C-T

105730186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7906129-C-G

105730186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7906129-C-T

http://identifiers.org/hco/13/GRCh38#105730195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7906137-C-A

105730195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7906137-C-T

105730354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7906377-G-A

105730412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7906668-G-T

105730418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7906674-A-G

105730419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7906675-G-T

105730489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7906739-G-T

105730518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7906765-C-T

105731229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7907461-T-C

http://identifiers.org/hco/13/GRCh38#105731461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7907658-C-A

105731541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7907736-C-G

105731541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7907736-C-T

105731671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7907865-C-T

105731761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7907959-G-A

105731941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7908141-C-T

105732096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7908293-T-A

105732177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7908372-T-C

105732265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7908481-C-G

http://identifiers.org/hco/13/GRCh38#105732286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7908502-C-A

105732286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7908502-C-T

105732323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7908539-A-G

105732399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7908590-C-T

105732403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7908594-G-A

105732559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7908750-T-C

http://identifiers.org/hco/13/GRCh38#105732649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7908840-C-A

105732830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7909024-T-G

105732898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7909102-T-C

105732905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7909112-G-A

http://identifiers.org/hco/13/GRCh38#105733417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7909646-C-A

105733433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7909662-T-A

105733507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7909705-C-T

105733686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7909877-T-C

105734122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7910247-A-G

105734139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7910264-T-A

105734139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7910264-T-C

105734319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7910443-G-A

105734333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7910456-T-A

105737973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7913041-G-A

105738176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7913199-T-C

105738492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7913520-T-A

105738632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7913657-C-T

105738648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7913673-G-T

105738901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7913892-T-G

105738915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7913906-A-G

http://identifiers.org/hco/13/GRCh38#105738935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7913926-C-A

105739060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7914049-G-T

105739143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7914154-A-T

105739270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7914277-C-T

105739474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7914436-A-G

http://identifiers.org/hco/13/GRCh38#105739695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7914658-C-A

105740572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7914975-G-T

105740581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7914984-T-C

105740615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7915018-T-C

105742647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7923056-T-C

http://identifiers.org/hco/13/GRCh38#105742752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7923164-C-A

105743099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7923449-T-G

105743111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7923462-C-T

http://identifiers.org/hco/13/GRCh38#105743173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7923517-C-A

http://identifiers.org/hco/13/GRCh38#105743233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7923561-A-C

105743233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7923561-A-G

105744828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7924272-T-C

105744905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7924350-T-A

105745344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7924758-G-T

105748554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7925105-A-G

105748795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7925315-A-G

105748831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7925368-G-C

105749128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7925868-G-A

105749128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7925868-G-C

105749181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7925911-A-G

105749181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7925911-A-T

105749183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7925913-C-T

105749478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7926188-A-G

105750079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7926762-A-T

105750148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7926832-A-G

http://identifiers.org/hco/13/GRCh38#105750218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7926888-C-A

105750239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7926913-A-G

105750389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7927042-C-T

105750696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7932445-A-T

105750869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7932643-A-G

105751529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7933270-T-A

105751629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7933363-C-T

105751687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7933414-A-G

105752103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7933814-C-T

105753319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7935386-T-G

105755146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7935500-A-G

105755373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7935745-A-T

105755439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7935814-T-C

105755907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7937142-A-G

105755907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7937142-A-T

105756267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7937483-A-G

105756267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7937483-A-T

105756402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7937727-T-C

105756432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7937768-C-T

105756546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7937889-T-C

105756817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7938178-T-A

105758175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7939448-C-T

105758330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7939586-G-A

105758874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7939833-C-T

105759895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7940868-A-G

105760525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7941372-T-C

105761039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7941887-T-C

http://identifiers.org/hco/13/GRCh38#105761041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7941889-C-A

105761041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7941889-C-T

105761063-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7941911-T-G

105761193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7942033-C-G

105763125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7943651-A-G

105763278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7943799-T-A

105763334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7943859-T-C

105763351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7943876-C-T

105764031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7944197-G-A

105764031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7944197-G-T

105764159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7944325-A-G

105764181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7944347-G-C

105764181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7944347-G-T

105764249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7944419-G-A

105764302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7944472-A-G

105764399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7944549-T-C

105764470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7944632-A-G

105768663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7952816-G-A

105768673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7952826-C-T

105768865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7952990-G-C

105769164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7953238-C-T

105769240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7953312-G-A

105769493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7953568-C-T

105769518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7953594-G-A

105769545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7953627-T-C

105769577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7953655-C-T

105769591-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7953669-A-T

105769603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7953681-G-C

105769994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7954062-C-G

105769994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7954062-C-T

105770030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7954087-A-G

105770075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7954133-C-T

105770328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7954372-T-C

105770371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7954399-G-T

105770480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7954481-G-A

105770544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7954546-T-A

105770587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7954589-C-G

105770655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7954652-A-G

105770787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7954777-G-A

105770972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7954957-G-A

105771143-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7955098-T-A

105771256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7955710-C-T

105771306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7955763-G-C

105771375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7955826-T-C

105771882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7956272-A-G

105772068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7956456-G-C

105772613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7956772-G-A

105772624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7956776-G-A

105772653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7956796-T-A

105772927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7957031-G-A

105772927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7957031-G-T

105773059-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7957181-C-G

105773140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7957255-G-T

105773335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7957444-A-G

105773604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7957697-C-T

105773643-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7957736-T-A

105773643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7957736-T-C

105773683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7957774-G-A

105773723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7957814-C-T

105773815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7957905-C-T

105773920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7958003-G-A

105773927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7958010-A-T

105774044-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7958116-A-T

105774099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7958157-C-T

105774173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7958231-G-A

105774279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7958309-C-G

105774331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7958341-A-G

http://identifiers.org/hco/13/GRCh38#105774374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#7958373-A-C

105774374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7958373-A-G

105774399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7958398-G-A

105774516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7958518-G-A

105775108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 7959099-T-G

105775272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7959719-C-T

105775451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7959903-G-A

105775451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7959903-G-T

105775543-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7959990-T-A

105775964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7960281-G-T

105776016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7960322-A-G

105776113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7960481-C-T

105776411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7960770-C-G

105776992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7961351-G-A

105777157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7961516-G-A

105777259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7961621-T-C

105777274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7961636-G-T

105777333-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7961696-T-G

105777474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7961808-C-T

105777542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7961859-T-C

105777583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7961889-T-C

105777652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7961943-G-A

105777947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7962218-C-T

105778096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7962408-T-C

http://identifiers.org/hco/13/GRCh38#105778150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7962507-C-A

105778739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7963231-G-A

http://identifiers.org/hco/13/GRCh38#105778913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7963373-C-A

http://identifiers.org/hco/13/GRCh38#105778914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7963374-C-A

105778914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7963374-C-G

105778946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7963405-A-G

105779061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7963517-A-G

105779083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7963538-T-A

105779389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7964021-C-T

105779408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7964040-C-T

105779435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7964076-T-C

105779516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7964178-C-G

105779704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7964339-A-G

105779884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7964522-A-G

105779906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7964541-T-C

105780312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7964889-G-A

105780383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7965010-T-C

105780453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7965083-T-A

105786427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7968229-G-A

105786427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7968229-G-T

http://identifiers.org/hco/13/GRCh38#105786573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7968389-C-A

105786724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7968540-C-T

105786934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7968740-C-T

http://identifiers.org/hco/13/GRCh38#105786947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7968758-C-A

105786947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7968758-C-T

105787182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7968996-G-A

105787298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7969115-G-A

105787336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7969159-A-G

105787336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7969159-A-T

105787376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7969199-T-C

105787427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7969246-T-C

105787456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7969275-T-C

105787614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7969421-C-G

105787631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7969445-A-G

105787764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7969577-A-G

105787911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7969723-G-A

105787911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7969723-G-T

105787926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7969738-C-T

105788455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7970282-T-A

105789152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7970936-G-C

105789166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7970953-G-A

105789227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7971013-G-A

105789758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7971426-G-T

105789774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7971432-G-A

105792829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7980823-G-A

105792829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7980823-G-T

105792840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7980838-G-T

105792876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7980873-G-C

105794484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7981194-G-A

105794599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7981311-G-T

105794743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7981535-G-C

105794870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7981658-T-G

http://identifiers.org/hco/13/GRCh38#105795107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7981890-A-C

105795235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7982011-G-A

http://identifiers.org/hco/13/GRCh38#105795438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#7982207-C-A

105795438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7982207-C-T

105795444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7982213-A-G

105795491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7982260-A-G

105795691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 7982621-G-A

105797271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: non coding transcript exon variant
orthologous variants: 7982817-G-A

105797342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: non coding transcript exon variant
orthologous variants: 7982885-T-G

105797374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42500
most severe consequence: non coding transcript exon variant
orthologous variants: 7982917-T-C