108713078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796880-G-A

108713142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796817-G-T

108713266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796669-G-A

108713326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796610-G-A

108713326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796610-G-T

108713357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796575-A-G

108713359-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796573-T-A

108713360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796572-T-C

108713372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796560-T-C

http://identifiers.org/hco/1/GRCh38#108713392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108796540-C-A

108713409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796523-A-G

108713424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796508-A-T

108713584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796353-T-C

108713628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796312-A-G

http://identifiers.org/hco/1/GRCh38#108713652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108796288-C-A

108713804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796162-T-C

108713888-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108796070-T-G

108713979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108795941-T-C

108714084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108795719-G-A

108714273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108795531-C-T

108715528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108794339-C-T

108715657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108794197-G-A

108715657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108794197-G-C

108715663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108794191-G-A

108715669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108794185-G-A

108715677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108794177-A-G

108715679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108794175-A-G

108715942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108793910-C-T

108716038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108793842-G-A

108716039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108793841-C-T

108716127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108793761-G-A

108716185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108793711-A-G

108716319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108793579-A-G

108716332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108793566-T-G

108716571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108793318-T-C

108716722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108793165-T-C

108716723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108793164-G-A

108716906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108792668-C-T

108716977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108792554-A-G

108717071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108792467-C-T

108717072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108792466-C-T

108717107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108792417-T-C

108717314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108792221-G-A

108717437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108792132-G-A

108717536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108792038-C-G

108717683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108791034-G-A

108717683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108791034-G-T

108717686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108791031-A-G

108717803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108790914-G-A

108717803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108790914-G-T

108718051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108790666-T-A

108718059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108790659-T-G

http://identifiers.org/hco/1/GRCh38#108718106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108790611-C-A

108718113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108790604-T-G

108718144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108790574-A-G

http://identifiers.org/hco/1/GRCh38#108718247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108790471-C-A

108718335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108790376-G-A

http://identifiers.org/hco/1/GRCh38#108718711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108788987-C-A

108718732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108788963-T-G

108718807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108788882-T-C

108718866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108788823-G-A

108718934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: synonymous variant
orthologous variants: 108788755-A-G

108718968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108788721-G-A

108719096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108788593-T-C

108719132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108788557-G-A

http://identifiers.org/hco/1/GRCh38#108719224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108788460-A-C

108719283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108788422-C-T

108719471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108788189-T-C

108719697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108787955-C-T

108719698-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108787954-A-T

108719996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108787622-G-T

108720027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108787592-T-C

108720055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: 108787564-C-T

108720156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108787459-T-G

108720544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: 108786237-T-C

108720834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108785953-C-G

108721683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108784841-G-T

108721935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108784511-C-T

108721964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108784482-C-T

108722183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108784135-G-A

http://identifiers.org/hco/1/GRCh38#108722209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108784113-C-A

108722209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108784113-C-T

108722231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108784090-A-G

108722238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108784082-G-C

108722238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108784082-G-T

http://identifiers.org/hco/1/GRCh38#108722263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108784057-A-C

108722263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108784057-A-G

108722269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108784051-G-A

108722269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108784051-G-T

108722469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108783873-A-G

http://identifiers.org/hco/1/GRCh38#108722610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108783732-A-C

108722643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108783697-T-C

http://identifiers.org/hco/1/GRCh38#108722691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108783648-A-C

108722691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108783648-A-G

108722691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108783648-A-T

108722742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108783241-T-C

108722752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108783231-A-G

108723138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108782329-G-A

108723365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108781953-A-G

108723472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108781857-G-T

108723653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108781685-T-C

108723658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108781680-G-A

108723743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108781607-T-C

108723845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108781526-G-A

108724358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108781085-G-A

108724417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108781029-A-G

108724417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108781029-A-T

108725538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779911-G-A

108725538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779911-G-T

108725569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779882-G-T

http://identifiers.org/hco/1/GRCh38#108725679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108779773-C-A

108725695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779757-G-T

108725802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: synonymous variant
orthologous variants: 108779632-G-A

108725863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108779571-G-A

108726024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779410-T-C

108726107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779394-T-C

108726122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779379-A-G

108726134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779368-C-T

http://identifiers.org/hco/1/GRCh38#108726141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108779361-C-A

108726206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779296-G-C

108726395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779108-G-A

108726460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779044-G-A

http://identifiers.org/hco/1/GRCh38#108726491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108779014-C-A

108726491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779014-C-G

108726495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779010-G-A

108726496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108779009-T-C

108726514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778991-G-A

108726517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778988-A-T

108726554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778955-T-G

108726574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778935-A-G

108726597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778898-G-A

108726597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778898-G-T

108726649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778840-G-A

108726655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778834-T-C

108726838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778616-T-C

108726881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778576-G-A

108726912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778554-A-G

108726953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778515-G-A

108727530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778303-G-A

108727622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778256-G-A

108727712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778172-G-T

108727740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778157-G-C

108727740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108778157-G-T

http://identifiers.org/hco/1/GRCh38#108727810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108778097-C-A

108727810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 108778097-C-G

108727840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: synonymous variant
orthologous variants: 108778067-T-C

108727925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108777982-A-T

108727994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108777913-A-G

108728090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777817-C-T

108728097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777810-G-A

108728114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777794-C-T

http://identifiers.org/hco/1/GRCh38#108728149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108777759-C-A

108728149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777759-C-G

108728149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777759-C-T

108728162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777739-A-G

http://identifiers.org/hco/1/GRCh38#108728191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108777648-C-A

108728191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777648-C-G

108728191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777648-C-T

108728235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777578-G-A

108728267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777542-G-A

108728275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777534-A-G

108728275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777534-A-T

108728291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777517-G-A

108728291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777517-G-T

108728490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777320-A-G

108728490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777320-A-T

108728506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777304-G-A

108728506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108777304-G-T

http://identifiers.org/hco/1/GRCh38#108728559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108776740-C-A

108728697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: stop gained
orthologous variants: 108776603-C-T

108728730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108776570-A-G

108728739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108776561-G-A

108728748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108776552-G-A

108728748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: stop gained
orthologous variants: 108776552-G-T

108728767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108776533-G-C

108728803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108776497-G-A

108728835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108776465-G-A

108728922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108776393-G-A

http://identifiers.org/hco/1/GRCh38#108728949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108776366-C-A

108728957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108776358-T-A

108728957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108776358-T-G

http://identifiers.org/hco/1/GRCh38#108728977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108776341-A-C

http://identifiers.org/hco/1/GRCh38#108729022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108776298-C-A

108729022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108776298-C-T

108729121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108776185-T-G

108729161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108776144-G-T

108729166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108776139-A-G

108729231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108776083-C-T

108729243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108776072-A-G

108729520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108775861-G-A

http://identifiers.org/hco/1/GRCh38#108729527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108775854-C-A

108730099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108775621-C-T

108730107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108775613-G-A

108730116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108775604-T-C

108730343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108775287-G-A

108730347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108775283-C-T

108730360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108775278-T-A

108730360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108775278-T-G

http://identifiers.org/hco/1/GRCh38#108730361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108775277-C-A

http://identifiers.org/hco/1/GRCh38#108730396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108775249-C-A

108730469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108775212-T-G

http://identifiers.org/hco/1/GRCh38#108730686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108774618-C-A

108730686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108774618-C-T

108730765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: synonymous variant
orthologous variants: 108774539-T-C

108730766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108774538-G-A

108730865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108774439-A-G

108730889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108774415-G-A

108730905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108774399-G-A

108730962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108773788-G-A

108730962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108773788-G-C

108730962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108773788-G-T

108730994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108773756-T-C

108730994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108773756-T-G

108731073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108773170-T-A

108731286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108772963-T-A

http://identifiers.org/hco/1/GRCh38#108731380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108772764-A-C

108731380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108772764-A-G

108731499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108772644-G-T

108732020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108770828-G-A

108733184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108770386-A-G

108733225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108770339-G-T

108733336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: stop gained
orthologous variants: 108770237-G-A

http://identifiers.org/hco/1/GRCh38#108733514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108770059-C-A

108733514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: missense variant
orthologous variants: 108770059-C-T

108733537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108770036-A-G

108733618-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108769047-A-T

108734295-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: 108768475-A-T

108734402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: 108768367-G-T

http://identifiers.org/hco/1/GRCh38#108734431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#108768338-A-C

108734455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: 108768315-G-A

108734548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: 108768228-T-C

108734610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: 108768167-G-A

108734610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: 108768167-G-T

108734614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: 108768163-G-T

http://identifiers.org/hco/1/GRCh38#108734645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#108768131-C-A

108734646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: 108768130-T-C

http://identifiers.org/hco/1/GRCh38#108734654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#108768122-C-A

108734654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron_variant, undefined
orthologous variants: 108768122-C-T

108737535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108766181-T-C

108737582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108766133-G-A

108737582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108766133-G-T

108737749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108765993-T-G

108737955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108765780-G-A

http://identifiers.org/hco/1/GRCh38#108737965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108765770-A-C

http://identifiers.org/hco/1/GRCh38#108737971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108765764-A-C

http://identifiers.org/hco/1/GRCh38#108740188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108765498-C-A

108740650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108764994-T-A

108740764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108764884-A-T

108740888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108764800-A-G

108740896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108764792-C-T

108741003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108764726-G-A

108741586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108763914-T-C

108741619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108763877-A-G

108741657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108763843-G-A

108741657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108763843-G-C

108741657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108763843-G-T

108741862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108763642-T-C

108741891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108763613-C-G

108741903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: intron variant
orthologous variants: 108763601-T-C

108741972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108763533-T-C

http://identifiers.org/hco/1/GRCh38#108741975-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108763530-A-C

108741976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108763529-G-T

108742011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108763501-T-C

108742033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108763479-G-C

108742033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108763479-G-T

http://identifiers.org/hco/1/GRCh38#108742067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108763447-C-A

108742067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108763447-C-T

http://identifiers.org/hco/1/GRCh38#108742182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108763328-C-A

108742209-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108763297-T-A

http://identifiers.org/hco/1/GRCh38#108742232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108763274-C-A

108742232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108763274-C-G

108742232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108763274-C-T

108742263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108763131-T-C

108742388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108763004-T-C

108742390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108763002-G-A

108742390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108763002-G-T

108742582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108762807-G-T

108742650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108762715-A-G

http://identifiers.org/hco/1/GRCh38#108742668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#108762699-C-A

108742668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108762699-C-T

108742705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26668
most severe consequence: 3 prime UTR variant
orthologous variants: 108762660-G-T