104939130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45364161-G-A

104939138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45364155-A-G

104939246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45364014-T-G

104939498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45363547-T-C

104940032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45363114-T-C

104940046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45363100-T-G

104940289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362885-G-T

http://identifiers.org/hco/6/GRCh38#104940292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45362882-A-C

104940292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362882-A-G

104940318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362856-T-C

104940362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362831-T-C

http://identifiers.org/hco/6/GRCh38#104940444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45362752-C-A

104940444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362752-C-T

104940446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362750-G-T

104940489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362694-G-C

104940489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362694-G-T

http://identifiers.org/hco/6/GRCh38#104940533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45362632-C-A

104940633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362531-C-T

104940634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362530-G-A

104940634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362530-G-T

http://identifiers.org/hco/6/GRCh38#104940792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45362458-C-A

104940792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362458-C-T

http://identifiers.org/hco/6/GRCh38#104940899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45362402-C-A

104940899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45362402-C-T

104940966-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45362364-T-A

104940966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45362364-T-C

http://identifiers.org/hco/6/GRCh38#104940989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45362344-C-A

104940989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45362344-C-T

http://identifiers.org/hco/6/GRCh38#104941007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45362326-C-A

104941007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 45362326-C-T

104941069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362265-G-A

104941069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362265-G-C

104941069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362265-G-T

104941163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362195-G-A

http://identifiers.org/hco/6/GRCh38#104941207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45362125-C-A

104941213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362119-G-A

104941224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45362108-T-G

104941369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45361996-G-A

104941369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45361996-G-T

104941633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45361805-C-G

104941674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45361762-A-G

104942042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45361437-T-C

104942166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45361313-C-G

104942441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45361020-G-A

104942570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45360903-A-G

104942767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45360688-A-G

104943125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45360328-A-G

http://identifiers.org/hco/6/GRCh38#104943182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45360277-C-A

104943397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45360049-T-A

104943421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45360025-T-C

104943599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45359877-A-T

104943768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45359716-T-C

104943819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45359663-A-G

104943841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45359641-A-G

104943841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45359641-A-T

104943842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45359640-T-C

104943899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45359585-T-A

104943971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45359525-A-G

104944112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45359408-G-A

http://identifiers.org/hco/6/GRCh38#104944538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45358983-A-C

http://identifiers.org/hco/6/GRCh38#104944653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45358867-A-C

104945210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45358037-A-G

104945599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45357694-A-T

104945709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45357602-T-C

104945852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45357447-A-G

104946159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45357197-T-C

104946392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45356987-T-G

104946486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45356899-A-G

104946670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45356747-A-G

http://identifiers.org/hco/6/GRCh38#104946688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45356729-C-A

104946688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45356729-C-T

104946694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45356718-C-T

104946940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45356527-T-C

104947081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45356383-T-C

104947545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45356251-T-C

http://identifiers.org/hco/6/GRCh38#104947643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45356157-A-C

http://identifiers.org/hco/6/GRCh38#104947796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45355920-C-A

104947796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45355920-C-T

104947803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45355908-G-A

104947873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45355682-C-T

104949325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45354029-A-G

104949477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45353914-A-T

104949536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45353857-A-G

104949579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45353715-G-A

104949790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45353489-G-A

104950218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45352726-A-G

104950356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45352594-A-T

104950428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45352523-A-G

104950428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45352523-A-T

104950622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45352364-A-G

104950783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45352215-G-T

104951569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45351367-T-C

104952328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45350734-T-C

104952354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45350710-A-T

104952480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45350559-A-G

104952480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45350559-A-T

104953629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45349569-T-C

104953912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45349274-A-G

http://identifiers.org/hco/6/GRCh38#104954025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#45349161-A-C

104954025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45349161-A-G

http://identifiers.org/hco/6/GRCh38#104954969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45348256-A-C

104954969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45348256-A-G

104955044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45348184-T-C

104955101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45348137-A-G

104955194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45348088-C-T

104955856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45347465-T-A

104956235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45347134-C-T

104956238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45347129-C-G

104956238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45347129-C-T

104956784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45346604-G-T

104956822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45346573-A-G

104956944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45346459-A-G

http://identifiers.org/hco/6/GRCh38#104957392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45346013-C-A

104957397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45346007-T-A

104957397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45346007-T-G

104957773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45345618-A-G

http://identifiers.org/hco/6/GRCh38#104958012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45345390-C-A

104958012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45345390-C-G

104958012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45345390-C-T

104958054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45345359-T-C

104958054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45345359-T-G

104958063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45345350-A-G

http://identifiers.org/hco/6/GRCh38#104958140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45345277-C-A

104958140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: missense variant
orthologous variants: 45345277-C-G

104958140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: missense variant
orthologous variants: 45345277-C-T

104958328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45345090-G-A

104958328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron_variant, undefined
orthologous variants: 45345090-G-T

104958574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45344844-T-C

104958574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45344844-T-G

104958822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45344609-A-G

104959360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45344095-T-C

104959367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45344088-T-C

104959426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45344035-C-T

104959552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45343921-T-A

104960118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45343387-C-T

104960341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45343210-G-A

104960352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45343201-G-A

104960353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45343200-G-A

http://identifiers.org/hco/6/GRCh38#104960395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45343161-A-C

104960776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45342089-T-C

104961012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45341886-T-G

104961131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45341769-T-C

104961363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45341563-A-G

104961883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45341148-A-G

104962319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45340740-A-G

104962713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45339868-G-A

104962892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45339630-C-T

104962901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45339600-A-G

104962910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45339587-T-C

104963266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45339144-T-C

104963342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45339046-G-A

104963342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45339046-G-T

http://identifiers.org/hco/6/GRCh38#104966084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45338164-A-C

104968631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45335560-T-C

104969140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45335116-A-G

http://identifiers.org/hco/6/GRCh38#104969209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45335047-A-C

http://identifiers.org/hco/6/GRCh38#104969211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45335045-A-C

104969211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45335045-A-G

104969707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45334667-A-T

104969886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45334497-C-G

104970267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45334138-A-G

104970810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45333501-A-G

104971626-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45332659-A-T

104973439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45331304-C-T

104973626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45331137-C-T

104973822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45330964-C-G

104974553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45330892-C-T

104974565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45330880-C-G

104974603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45330842-G-A

104978429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45328330-C-T

104979870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45323978-G-T

104979983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45323832-G-A

104979983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45323832-G-T

104980124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45323570-C-T

104980151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45323465-G-A

104980454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45323201-C-T

104980833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45322823-T-C

104980833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45322823-T-G

104980975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45322677-A-G

104980993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45322659-T-C

104981087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45322560-G-A

104981104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45322541-T-G

104981170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45322476-A-G

104981184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45322462-C-T

104981231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45322412-T-C

http://identifiers.org/hco/6/GRCh38#104981469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45322169-C-A

104981629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45322025-G-A

104981673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45321965-A-G

104981679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45321959-G-T

104998580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45315484-C-G

105024701-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45299627-G-C

105025046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45298347-C-G

105025058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45298335-C-G

105025227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45298147-C-T

http://identifiers.org/hco/6/GRCh38#105025533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45297869-A-C

105025555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45297853-C-G

105025555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45297853-C-T

105025715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45297634-C-T

105026452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: missense variant
orthologous variants: 45296648-C-T

http://identifiers.org/hco/6/GRCh38#105026589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45296510-C-A

105026589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45296510-C-T

105026592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45296507-T-C

105026854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45296281-C-T

105027130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45296102-C-G

105027344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45295917-G-A

105027344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45295917-G-T

105027390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45295881-T-C

105028351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45295466-G-A

105028605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45295217-A-G

105028704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45295125-C-T

105028809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45295061-T-C

105028878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45295027-C-G

http://identifiers.org/hco/6/GRCh38#105028892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45295013-C-A

105029229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45294734-A-G

105029243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45294732-G-A

105029481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45294550-A-G

105029505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45294527-G-A

105029521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45294519-A-G

105029531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45294510-T-C

105031936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45291045-C-T

105031942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45291039-C-T

105032299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45290660-T-C

105032344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45290632-G-A

105032365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45290612-T-A

105032598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45290532-C-T

105032658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45290527-G-A

105032862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45290412-A-G

105033029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45290243-A-G

105033701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45289621-A-G

105034064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45289297-T-C

105034152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45289206-A-G

105034152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45289206-A-T

105034751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45288641-A-G

105034894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45288516-A-G

105035095-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45288334-T-G

105035843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45287634-T-C

105035964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45287510-A-G

105035970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45287504-T-G

105036113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45287338-T-C

105036332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45287159-G-A

http://identifiers.org/hco/6/GRCh38#105036928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45286600-C-A

http://identifiers.org/hco/6/GRCh38#105037025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45286486-C-A

105037138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45286385-A-G

105037253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45286307-C-T

http://identifiers.org/hco/6/GRCh38#105037286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45286277-C-A

105041899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45284701-T-C

105041963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45284653-A-G

105042223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45284424-A-G

http://identifiers.org/hco/6/GRCh38#105042280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45284357-A-C

105042328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45284287-T-C

105042357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45284258-T-C

105042638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45283947-T-G

105042743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45283848-C-T

105042774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45283815-T-G

105056548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45274652-T-C

105064780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45268248-T-C

105064780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45268248-T-G

http://identifiers.org/hco/6/GRCh38#105066287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45266847-C-A

105066288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45266846-G-A

http://identifiers.org/hco/6/GRCh38#105067114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45265612-A-C

105067614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45265140-C-T

105068042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45264546-G-T

http://identifiers.org/hco/6/GRCh38#105068364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45264243-C-A

105068598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45264028-T-C

105069873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45263281-A-G

http://identifiers.org/hco/6/GRCh38#105069880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45263274-C-A

105070255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45263039-T-C

105070268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45263025-C-G

105070354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45262943-G-A

http://identifiers.org/hco/6/GRCh38#105074593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45261514-A-C

http://identifiers.org/hco/6/GRCh38#105075850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45260528-A-C

105075981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45260402-T-C

105076297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45260135-G-T

105076315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45260117-T-G

105076546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45259893-T-C

105077587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45259506-G-A

105077596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45259487-T-C

http://identifiers.org/hco/6/GRCh38#105077691-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45259399-A-C

http://identifiers.org/hco/6/GRCh38#105077704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45259386-C-A

105077706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45259384-A-T

http://identifiers.org/hco/6/GRCh38#105078131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45257834-C-A

105078131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45257834-C-G

105078225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45257749-C-T

105078317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45257668-T-A

105078317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45257668-T-C

105078329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45257656-T-C

105078329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45257656-T-G

105078362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: intron variant
orthologous variants: 45257587-T-C

105078433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: missense variant
orthologous variants: 45257506-C-G

105078433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: missense variant
orthologous variants: 45257506-C-T

105078466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: missense variant
orthologous variants: 45257473-C-T

105078549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: synonymous variant
orthologous variants: 45257390-C-T

105078598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: missense variant
orthologous variants: 45257341-A-G

http://identifiers.org/hco/6/GRCh38#105078636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45257303-A-C

105078636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: synonymous variant
orthologous variants: 45257303-A-G

105078711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: synonymous variant
orthologous variants: 45257231-C-T

http://identifiers.org/hco/6/GRCh38#105079029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45256935-C-A

105079029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45256935-C-T

105079070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45256895-G-A

105079070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45256895-G-T

http://identifiers.org/hco/6/GRCh38#105079075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45256882-C-A

105079075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45256882-C-T

105079101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45256841-A-T

105079471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45256430-G-T

105079599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45256301-G-T

105079687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45256218-T-C

http://identifiers.org/hco/6/GRCh38#105080098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45255828-C-A

105080098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45255828-C-T

105080296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45255623-T-C

105080407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45255532-C-T

105080917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45255112-C-T

105080947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45255082-A-G

http://identifiers.org/hco/6/GRCh38#105081695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45254319-C-A

105081728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45254285-A-G

105081752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45254261-G-T

105081753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45254260-G-C

105081806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45254215-G-A

105081806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45254215-G-T

105081829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45254193-G-A

http://identifiers.org/hco/6/GRCh38#105081853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#45254168-C-A

105081861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45254159-C-T

105082301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45253728-T-A

105082772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45253263-G-T

105082916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32207
most severe consequence: 3 prime UTR variant
orthologous variants: 45253116-C-G