http://identifiers.org/hco/2/GRCh38#109129283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#58649114-C-A

109129283-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58649114-C-G

109129283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58649114-C-T

109129369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58649207-G-A

109129421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58649270-G-A

109129421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58649270-G-C

109129421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58649270-G-T

109129432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 58649281-G-A

109129570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 58649426-A-G

http://identifiers.org/hco/2/GRCh38#109130019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#58649854-C-A

109130019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 58649854-C-T

109130035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 58649870-T-C

http://identifiers.org/hco/2/GRCh38#109130065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#58649900-C-A

109130065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 58649900-C-G

109130065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 58649900-C-T

109130155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58649989-G-A

109130155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58649989-G-T

109130356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58650324-C-T

109130712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58650705-A-G

109130739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58650732-G-T

109131516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58651840-G-A

109131601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58651919-C-T

109131606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58651924-G-A

109131725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58652044-G-A

http://identifiers.org/hco/2/GRCh38#109131865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58652298-C-A

109131865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58652298-C-G

109131865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58652298-C-T

109132169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58652670-T-G

109132173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58652716-A-G

109132399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58652919-G-T

109133033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58653681-G-A

109133094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58653718-G-A

109133229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58653848-G-C

109134621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58654595-G-A

109134827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58654766-G-C

109134943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58654880-G-A

109134980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58654912-C-T

109135090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58655000-G-A

109135106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58655016-G-A

109135242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58655129-A-G

109135332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58655225-G-A

109135383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58655302-C-G

109135388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58655307-C-T

109135399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58655317-G-A

109135670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58655518-G-C

109135724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58655574-A-G

109135754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58655604-C-T

109135835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58655684-C-T

109136215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58656114-T-C

109136415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58656312-C-G

109136415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58656312-C-T

109136418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58656315-G-A

http://identifiers.org/hco/2/GRCh38#109136555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58656541-A-C

109136579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58656603-C-T

http://identifiers.org/hco/2/GRCh38#109136670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#58656762-C-A

109136670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58656762-C-T

109136786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58656873-G-C

109136873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58656944-C-G

109137022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58657048-G-A

109137193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58657358-G-T

http://identifiers.org/hco/2/GRCh38#109137393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58657647-A-C

109137438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58657696-G-C

109137787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58658043-C-T

109138594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58658825-C-T

109139944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58658951-G-A

109139974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58658978-T-A

109139974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58658978-T-C

109140098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58659102-C-T

109140191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58659190-C-T

http://identifiers.org/hco/2/GRCh38#109140310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58659771-A-C

109140310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58659771-A-G

109140348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58659809-T-C

109140827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58659963-G-A

109140855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58659987-C-T

109140993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58660103-C-T

109141187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58660304-C-T

http://identifiers.org/hco/2/GRCh38#109141244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58660361-A-C

109141312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58660431-T-C

109141366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58660453-A-G

109141384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58660471-G-T

109141387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58660474-G-A

http://identifiers.org/hco/2/GRCh38#109141398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58660485-C-A

http://identifiers.org/hco/2/GRCh38#109141404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58660491-C-A

109141404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58660491-C-T

109141418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58660505-C-T

http://identifiers.org/hco/2/GRCh38#109141468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58660557-A-C

109141587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58660672-C-T

109141719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58660738-A-G

109141739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58660739-C-G

109141838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58660798-C-T

109141936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58660878-T-G

109142299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58661207-T-A

109146127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58662644-T-C

109146212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58662721-A-G

109146330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58662825-G-A

109146369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58662864-A-G

109146404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58662887-A-G

109146727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58663182-C-T

109146805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58663952-T-C

109146842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58663998-T-A

109146842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58663998-T-C

109146842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58663998-T-G

http://identifiers.org/hco/2/GRCh38#109146867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58664023-C-A

109146867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664023-C-T

109146871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664027-T-A

109146871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664027-T-C

http://identifiers.org/hco/2/GRCh38#109146875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58664031-C-A

109146875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664031-C-T

http://identifiers.org/hco/2/GRCh38#109146892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58664051-C-A

109146892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664051-C-G

109146892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664051-C-T

109146949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664080-T-C

109147073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664180-C-T

109147195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664293-C-T

109147246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664341-T-G

109147295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664378-C-G

109147301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664382-A-G

109147349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664427-C-G

109147479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664537-A-G

109147614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664680-C-T

109147636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664702-C-T

109147839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58664901-G-A

109147937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58665014-G-C

109148091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58665149-G-A

109148091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58665149-G-C

http://identifiers.org/hco/2/GRCh38#109148375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58665398-A-C

109148711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58665712-G-A

109148758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58665757-T-C

109148857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58665831-G-T

109149344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58666241-A-G

109149634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58666558-A-T

109150766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58668672-T-A

109150950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58668869-G-T

109150970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58668901-G-A

109150970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58668901-G-T

109151192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58669094-T-C

109151192-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58669094-T-G

109151197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58669097-C-G

109151513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58669427-T-C

109151666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58669580-C-T

109151811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58669718-C-T

109152305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58670245-A-G

109152468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58670581-C-G

109152653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58670761-A-G

109152756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58670840-G-T

109152788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58670867-C-G

109152839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58670934-A-G

109152905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58670992-C-G

109152905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58670992-C-T

http://identifiers.org/hco/2/GRCh38#109153109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58671125-C-A

109153111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58671127-C-T

109153176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58671184-T-C

109153176-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58671184-T-G

109153368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58671328-G-A

109153392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58671357-G-A

109153641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58671579-A-G

109153807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58671777-T-C

109154111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58672090-C-T

109154113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58672092-C-T

109154490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58672382-C-T

http://identifiers.org/hco/2/GRCh38#109154492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58672384-C-A

109154492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58672384-C-T

109154558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58672453-G-A

109163734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58673414-A-G

109163960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58673625-C-T

109165067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58675355-C-T

109165197-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58675489-T-G

109165240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58675529-T-C

109165283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58675573-G-A

109165320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58675605-C-T

109165402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58675682-A-T

109165460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58675733-G-T

109165568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58675852-C-T

109165649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58675925-G-A

109171996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58677760-G-A

109171996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58677760-G-T

http://identifiers.org/hco/2/GRCh38#109172020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58677782-A-C

109172020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58677782-A-G

109172057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58677814-G-C

109172075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58677832-A-G

109172137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58677890-G-A

109172500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58678158-A-G

http://identifiers.org/hco/2/GRCh38#109172646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58678283-A-C

109172647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58678284-A-G

109172652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58678289-T-C

109172653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58678290-T-C

109172775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58678424-G-T

109172817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58678467-A-T

109172929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58678564-C-G

109173249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58678859-A-G

http://identifiers.org/hco/2/GRCh38#109173376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58678945-C-A

109173376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58678945-C-T

109173452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58679016-T-C

109173469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58679036-C-G

109173508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58679089-G-A

109173947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58679219-T-C

109174958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58680971-G-A

109174958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58680971-G-C

109175421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58681883-T-C

109175513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58681930-G-A

109175551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58681968-C-T

109176044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58682137-C-T

109176067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58682160-G-A

109178218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58682467-T-A

109178220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58682469-G-A

109178430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58682665-G-A

109178531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58682766-C-T

109178597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58682809-C-T

http://identifiers.org/hco/2/GRCh38#109178599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58682811-A-C

109178599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58682811-A-G

109178691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58682900-A-G

109178701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58682910-G-A

109178732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58682941-A-G

109178737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58682946-T-C

109179003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58683215-A-G

109179390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58683689-G-T

109180851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58684169-A-G

109180944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58684254-T-C

109180961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58684266-C-T

109180963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58684268-C-G

109181175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58684456-T-A

109181257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58684532-C-G

109181522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58685378-G-A

109181562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58685418-C-G

109181915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58685660-G-C

http://identifiers.org/hco/2/GRCh38#109181943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58685694-C-A

109181981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58685728-C-T

109182563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58686024-A-G

109182702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58686143-A-G

109182756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58686197-C-T

109182933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58686432-G-A

109183554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58686666-G-A

109183554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58686666-G-T

http://identifiers.org/hco/2/GRCh38#109183573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58686685-C-A

109184112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687182-C-T

109184114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687184-T-C

109184219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687257-C-G

109184285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687315-C-G

109184313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687344-A-T

109184370-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687391-G-C

109184401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687421-A-T

109184436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687449-T-C

109184572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687545-A-G

109184704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687630-C-T

109184719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687640-C-T

109184723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687644-T-C

109185084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687918-G-A

109185089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687923-G-T

109185143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58687962-C-G

109185238-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58688057-T-G

109185616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58688411-C-T

109185654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58688450-C-T

109185658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58688454-G-A

109185686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58688482-T-C

109185692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58688488-T-A

109185750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58688544-G-A

109185823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58688611-G-A

109185874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58688662-A-G

109185900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58688676-G-A

109185926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58688694-C-T

109186123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58688889-C-G

109186138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58688904-G-T

http://identifiers.org/hco/2/GRCh38#109186214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58688973-C-A

109186214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58688973-C-T

109186456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58689205-C-T

109186476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58689226-C-G

109186476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58689226-C-T

109186518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58689265-G-C

109186556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58689304-C-G

109186679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58689413-T-A

109187280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58690111-C-G

109188067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58690266-G-A

109188120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58690328-A-T

109188126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58690334-C-T

109188215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58690410-G-C

109188286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58690471-T-A

109188711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58690847-G-A

109188796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58690915-A-G

http://identifiers.org/hco/2/GRCh38#109188798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58690917-C-A

109189006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58691117-C-T

109189077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58691196-C-G

109189327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58691445-C-T

109189950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58691858-T-C

109190524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58692166-G-A

109190648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58692292-A-G

109190691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58692334-T-G

109190733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58692375-T-G

109192407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58692923-C-T

109192585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58693191-G-A

109192647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58693248-A-G

109192762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58693364-A-G

109193201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58693782-C-T

109193333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58693918-G-A

109195205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58699565-G-T

109195406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58699702-C-T

109195596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58699877-A-G

109195768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58700008-T-G

109196111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58700323-C-T

109196185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58700371-T-A

109196226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58700412-G-A

109196323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58700513-C-T

109196629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58700780-G-A

109196656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58700804-G-A

109196729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58700877-G-A

109196753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58700903-C-T

109196826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58700987-A-G

109196832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58700993-C-T

http://identifiers.org/hco/2/GRCh38#109196900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58701042-A-C

109196900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58701042-A-T

http://identifiers.org/hco/2/GRCh38#109197046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58701169-C-A

109197250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58701461-G-A

109197265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58701476-G-A

109197301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58701503-G-A

109197614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58701760-A-G

109197671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58701812-G-T

109198223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58702995-G-A

109198648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58703389-G-A

109198690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58703432-T-C

http://identifiers.org/hco/2/GRCh38#109198708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58703456-A-C

109198730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58703470-C-G

109198730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58703470-C-T

109202822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58704294-C-T

109202823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58704295-G-A

109203065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58704506-G-A

109203224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58704641-C-T

109203274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58704677-G-A

109203325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58704699-C-T

109205985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58707015-A-G

109206172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58707206-C-T

109206998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58707375-G-A

109207018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58707395-G-A

109207018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58707395-G-C

109207129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58707509-A-G

109207159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58707543-G-A

109207658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58708065-G-C

109207660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58708067-G-T

109207716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58708119-A-G

109207733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58708137-G-T

109207764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58708160-A-G

109207810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58708205-A-G

http://identifiers.org/hco/2/GRCh38#109208170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58708537-C-A

109208170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58708537-C-T

109208187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58708554-C-G

109208370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58708890-G-A

109208374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58708894-G-C

109208432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58708935-G-A

109208458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58708961-A-G

109208515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58709019-T-A

109208548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58709050-A-G

109208587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58709109-C-T

109209030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58709596-G-T

109209058-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58709621-C-G

109209198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58709851-G-A

109209264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58709910-C-G

109209293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58709933-G-A

109209374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58710021-G-A

109209376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58710023-T-C

109209758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58710272-G-T

109209781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58710295-T-C

109209791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58710305-G-A

109210009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58710522-T-A

109210091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58710603-A-T

109210127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58710638-G-A

http://identifiers.org/hco/2/GRCh38#109210183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58710686-C-A

109210248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58710761-T-A

109210309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58710819-G-C

109210394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58710893-G-A

http://identifiers.org/hco/2/GRCh38#109210489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58712739-A-C

109210568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58712828-C-T

109210791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58712964-C-T

109210793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58712966-T-C

109210846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58713016-A-G

109211100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58713252-A-G

109211224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58713358-G-A

109211255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58713370-G-T

109211489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58713594-G-A

109211491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58713596-T-C

109212059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58713823-G-A

109212059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58713823-G-C

109212253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58714013-C-T

109212317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58714095-G-C

109218402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58716425-A-G

109228115-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58716912-C-G

109228117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58716914-A-G

109228151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58716938-T-C

109228259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58717047-G-A

109228453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58717203-T-C

109228453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58717203-T-G

109228767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58717473-C-G

109228767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58717473-C-T

109228768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58717474-T-G

109228794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58717500-G-A

109230850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58721144-C-G

109230933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58721219-A-G

109230933-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58721219-A-T

109231108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58721388-T-A

109231108-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58721388-T-G

109231155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58721431-C-T

109231175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58721450-G-A

109231175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58721450-G-T

109231206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58721486-C-G

109231287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58721574-G-T

109231811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58722046-A-G

109231884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58722120-G-A

109232027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58722268-G-A

109232054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58722295-G-A

http://identifiers.org/hco/2/GRCh38#109232244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58722477-A-C

109232266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58722490-C-T

109232309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58722530-G-C

109232765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58722955-A-G

109232776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58722966-G-A

109235596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58723532-C-T

109235646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58723568-G-A

109235668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58723590-A-G

109235677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58723597-G-A

109236258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58724030-A-G

109236346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58724134-G-A

109236347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58724135-T-G

109236349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58724137-T-C

109236657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58724557-T-C

109236854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58724758-C-T

109236857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58724761-C-T

109238238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58725092-C-G

109238311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58725166-A-G

109238376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58725232-A-G

109238379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58725235-T-C

http://identifiers.org/hco/2/GRCh38#109238879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58726050-A-C

109238974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58726145-G-C

109238974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58726145-G-T

109239097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58726258-A-G

109239253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58726422-G-A

109239345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58726516-A-G

109239485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58726640-G-A

109239553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58726707-C-T

109239569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58726734-A-G

109239599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58726771-A-G

109239689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58726844-A-G

109239836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58726985-C-T

109240198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58727299-A-T

109240683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58727640-G-A

http://identifiers.org/hco/2/GRCh38#109240697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58727648-C-A

109240772-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58727728-T-G

109240787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58727740-C-T

109240858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58727766-G-C

109240858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58727766-G-T

109240942-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58727813-C-G

http://identifiers.org/hco/2/GRCh38#109240985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58727856-C-A

http://identifiers.org/hco/2/GRCh38#109241055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58727913-A-C

109241075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58727933-G-A

109241080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58727938-A-G

109241180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58728032-T-A

109241205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58728057-C-G

109246014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58731118-G-A

109246251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58731386-C-G

109246378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58731691-G-A

109246643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58732060-G-A

109246643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58732060-G-C

109246643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58732060-G-T

109246648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58732065-T-A

109246670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58732077-G-A

109246694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58732101-C-T

109246961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58732284-T-G

109247247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58732572-A-G

109247279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58732600-C-T

http://identifiers.org/hco/2/GRCh38#109247447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58732748-C-A

109247447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58732748-C-G

109247447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58732748-C-T

109247723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58732909-T-G

http://identifiers.org/hco/2/GRCh38#109247950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58733098-C-A

109247950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58733098-C-T

109250177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58733511-A-G

109250297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58733629-C-T

109250342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58733676-T-C

109250385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58733720-T-G

109250579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58733914-A-G

109252306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58735375-A-T

109252364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58735433-G-C

109252364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58735433-G-T

109252500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58735579-C-T

109255155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58738927-C-T

109255223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58738998-C-T

109255228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58739003-G-A

109255267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58739036-G-C

109255298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58739063-C-T

109255495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58739254-T-G

109255547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58739306-A-G

http://identifiers.org/hco/2/GRCh38#109255599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58739357-A-C

109255669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58739425-A-G

109255679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58739435-C-T

109255736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58739481-T-C

109255747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58739492-G-C

http://identifiers.org/hco/2/GRCh38#109255850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58739595-A-C

109256547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58740904-G-A

109256554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58740916-T-A

109256608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58740973-G-A

109256674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58741044-T-C

109256927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58741224-G-A

109257089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58741346-G-C

109257104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58741352-G-A

109257322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58741559-G-A

109257732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58742274-G-T

http://identifiers.org/hco/2/GRCh38#109257784-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58742326-A-C

109257813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58742355-G-A

109257982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58742642-T-C

109257997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58742681-C-T

109258005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58742735-T-A

109258005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58742735-T-C

109258020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58742764-G-A

109258166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58742918-C-T

109258328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58743065-A-G

109266358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58747191-T-G

109266406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58747234-A-G

109266539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58747345-A-G

109266566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58747375-G-A

109266787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58747567-C-T

109266872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58747656-C-T

109266965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58747736-A-T

109267322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58748121-C-G

109269061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58749460-C-T

109269096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58749497-A-G

109269221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58749612-T-C

109269268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58749658-C-G

109269313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58749703-A-G

109269336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58749723-C-T

109269413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58749826-C-T

109270245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58751002-G-C

109270319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58751064-C-G

109270319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58751064-C-T

109270354-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58751088-G-C

109270458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58751198-T-C

109270740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58751447-T-G

109270781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58751486-G-T

109271357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58752403-A-G

109271521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58752547-T-C

109271621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58752661-G-A

109271697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58752727-A-G

109271728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58752760-T-C

109271763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58752792-T-C

109271763-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58752792-T-G

109271765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58752794-G-A

109271903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58752917-G-A

109272099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58753101-A-T

109272193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58753195-C-G

109272289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58753286-T-C

109272316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58753316-G-A

109272687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58753750-C-T

109272852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58753950-G-A

109272909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58754012-C-G

109273034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58754113-T-G

109273795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58754863-C-T

109273837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58754904-T-C

109273872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58754945-A-G

109273917-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58754988-T-A

109273917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58754988-T-C

109273978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58755046-T-C

109274003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58755067-A-G

109274003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58755067-A-T

109274113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58755176-G-A

109274403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58755586-G-A

109274405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58755588-G-A

109274405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58755588-G-C

109274637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58755752-C-G

109275451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58757915-G-A

109275514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58757966-G-T

109275567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58758013-G-A

109275576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58758019-A-T

109275595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58758039-G-T

109275707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58758150-C-T

109275714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58758158-C-T

109275870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58758318-T-C

109275961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58758409-A-G

109275971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58758418-G-A

109276050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58758477-C-T

109276309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58758780-A-G

109276361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58758832-G-A

109276469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58759717-T-C

109276567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58759803-G-T

109276687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58759908-G-C

109276718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58759945-T-C

109277124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58761869-G-A

109277279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58762034-C-T

109277422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58762172-A-G

109280407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58762943-G-A

109280466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58762999-G-T

109280589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58763112-G-T

109280599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58763122-T-A

109280599-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58763122-T-G

109280706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58763221-G-C

http://identifiers.org/hco/2/GRCh38#109280744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58763259-A-C

109280744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58763259-A-G

109280769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58763284-G-T

109280864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58763379-A-G

109280999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58763510-C-T

109281047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58763558-G-A

109281047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58763558-G-T

109281522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58763968-A-G

109281857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764239-C-T

109281952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764351-A-G

109281953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764352-G-C

109281983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764364-C-T

109282092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764471-C-G

109282268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764727-G-T

http://identifiers.org/hco/2/GRCh38#109282309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58764768-A-C

109282309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764768-A-G

109282310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764769-T-C

109282310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764769-T-G

109282343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764803-A-G

http://identifiers.org/hco/2/GRCh38#109282350-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58764810-A-C

109282395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764856-A-G

109282395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764856-A-T

109282542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764977-C-T

109282559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58764996-G-T

109282610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58765050-C-T

109282659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58765098-G-T

109282799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58765232-C-T

109282824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58765266-G-A

109282883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58765337-G-C

109283054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58765482-G-A

109283096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58765524-G-A

109283383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58765803-T-A

109283448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58765875-G-C

109283571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58765960-G-A

109283571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58765960-G-C

109283688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58766053-T-C

109283863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58766249-G-A

109283880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58766267-T-C

109283897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58766284-C-T

109284285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58766868-T-C

109284405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58766971-G-A

109284436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58767009-A-G

109284470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58767042-G-A

109284581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58767160-G-A

109284581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58767160-G-T

http://identifiers.org/hco/2/GRCh38#109284623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58767201-A-C

109284623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58767201-A-G

109284686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58767271-A-T

109284695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58767280-C-G

109284786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58767319-T-C

109284900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58767415-T-C

109284956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768011-G-A

109285018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768076-G-T

109285060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768115-A-G

109285131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768173-G-A

109285155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768193-A-G

109285176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768207-G-A

109285197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768226-G-A

109285197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768226-G-C

109285455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768481-T-A

109285593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768598-A-T

109285638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768640-T-G

109285652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768654-C-G

109285673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768675-A-T

109285910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58768856-G-C

109286128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58769057-G-C

http://identifiers.org/hco/2/GRCh38#109286391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58769287-C-A

109286391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58769287-C-G

109286398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58769294-C-G

109286779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58769939-G-T

109286843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58769990-C-T

109287027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58770124-G-A

109287055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58770155-T-G

http://identifiers.org/hco/2/GRCh38#109287198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58770306-C-A

109287309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58770425-G-C

109287309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58770425-G-T

109287402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58770513-G-A

109287728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58771033-A-T

109287805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58771109-C-T

109287807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58771111-A-T

109287873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58771174-C-T

109287930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58771219-C-G

109287998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58771286-G-A

109288187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58771461-C-T

109288321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58771585-C-T

109288955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58772214-A-T

109289060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58772315-T-C

109289224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58772466-G-T

109289239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58772481-G-A

109291040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58772992-G-A

109291188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58773126-T-C

109291263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58773202-A-T

109291265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58773204-G-A

109291282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58773349-T-C

109292468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58774172-T-C

109301151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58775306-G-C

109301255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58775439-C-T

109301259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58775443-C-T

109301281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58775465-G-A

109301346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58775544-G-A

109301592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: -G-A

109301732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: -A-G

109311842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58777400-A-G

109312079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58777694-G-A

109312107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58777767-T-C

109312107-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58777767-T-G

109312112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58777772-C-T

109312158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58777816-A-G

109316113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58779861-A-G

109316173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58779941-G-A

109316189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58779949-G-A

109316232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58779985-C-G

109316264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58780016-A-T

109316439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58780168-A-T

http://identifiers.org/hco/2/GRCh38#109317877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58780604-C-A

109318001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58780694-C-G

109318001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58780694-C-T

109318002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58780695-G-A

109318004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58780697-A-T

109318076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58780778-A-G

109318078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58780780-G-A

109318078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58780780-G-T

109318342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58781034-C-T

109318435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58781127-C-T

109318756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58781412-C-T

http://identifiers.org/hco/2/GRCh38#109318760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58781418-C-A

109318797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58781454-C-G

109318880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58781492-T-G

http://identifiers.org/hco/2/GRCh38#109318980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58781588-C-A

109319080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58781690-T-C

109319126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58781734-C-T

109319202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58781916-A-T

109319203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58781917-T-C

http://identifiers.org/hco/2/GRCh38#109319259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58782011-A-C

109319352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58782255-G-A

109319353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58782256-A-G

109319529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58782426-G-A

109319714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58782611-G-A

109319715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58782612-G-C

109320740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58784180-G-A

109320806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58784243-A-G

109320994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58784375-C-G

109321006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58784387-A-G

http://identifiers.org/hco/2/GRCh38#109321080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58784438-C-A

109321112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58784473-G-A

109321179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58784528-C-T

109321247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58784583-A-G

109321271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58784606-C-T

109321302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58784636-G-T

109321394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58784725-T-A

109321509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58784838-G-A

109322136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58785446-T-G

109322157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58785473-C-T

109322578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58785796-A-T

109322639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58785836-T-G

http://identifiers.org/hco/2/GRCh38#109322675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58785872-A-C

109322675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58785872-A-T

109323615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58786721-C-T

109324076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58787137-G-A

109324157-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58787220-T-G

109324163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58787228-A-G

109325000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58796094-G-A

109325169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58796238-G-A

109325169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58796238-G-T

109325348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58796417-T-C

http://identifiers.org/hco/2/GRCh38#109325364-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58796436-C-A

109335785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58804836-G-C

109335902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58804930-T-G

109336483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58805435-C-T

109336760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58805650-A-G

109336808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58805699-A-G

109338280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58806739-G-A

109338309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58806796-T-G

109338331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58806818-A-G

109338334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58806821-A-T

109339343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58807108-G-A

109339547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58807318-G-A

109339547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58807318-G-T

109339632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58807402-C-T

109339752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58807526-G-A

109340037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, undefined
orthologous variants: 58807786-T-G

http://identifiers.org/hco/2/GRCh38#109340055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58807803-A-C

109340207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58807948-T-C

109340298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58808041-T-A

109340311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58808060-G-A

109340311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58808060-G-T

109340339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58808088-C-T

109340373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58808112-G-A

http://identifiers.org/hco/2/GRCh38#109340419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58808165-A-C

109340524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58808285-G-C

109340614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58808364-G-A

109340623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58808372-G-A

109340627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58808376-C-T

109340816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58808561-C-T

109340820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58808565-C-G

109340857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58808597-G-A

109340862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58808602-A-G

109341497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58811129-C-T

109341559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58811196-T-G

http://identifiers.org/hco/2/GRCh38#109341564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58811201-A-C

109341564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58811201-A-G

http://identifiers.org/hco/2/GRCh38#109342721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58815265-C-A

109342758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58815297-C-T

109342889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58815430-G-A

109342913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58815454-G-A

109342923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58815464-C-G

109342985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58815518-G-A

109343169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58815674-T-A

109344118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58816124-G-T

109344266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58816251-G-C

109345121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58817580-G-A

109345121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58817580-G-T

109345146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58817617-G-A

109345248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58817715-G-C

109345322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58817767-C-T

109345355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58817800-T-C

http://identifiers.org/hco/2/GRCh38#109345430-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58817867-A-C

109345490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58817927-T-A

http://identifiers.org/hco/2/GRCh38#109345519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58817962-A-C

109345723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58818165-G-A

109345727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58818169-A-G

109345924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58818347-C-T

109345925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58818348-G-A

109345970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58818395-T-G

109346102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58818527-C-G

109346139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58818564-C-T

http://identifiers.org/hco/2/GRCh38#109346461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58818845-C-A

109346461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58818845-C-T

109346672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58819026-A-G

109346675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58819029-A-G

http://identifiers.org/hco/2/GRCh38#109347436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58819529-A-C

109347443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58819536-T-C

109347463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58819561-G-A

109347467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58819565-G-A

109347515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58819613-C-T

http://identifiers.org/hco/2/GRCh38#109347525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58819623-C-A

109347571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58819660-G-C

109347571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58819660-G-T

http://identifiers.org/hco/2/GRCh38#109347583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58819672-C-A

109347583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58819672-C-T

http://identifiers.org/hco/2/GRCh38#109347584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58819673-C-A

109347584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58819673-C-G

109347621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58819691-G-A

109347621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58819691-G-T

109347659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58819729-G-A

109347965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58820034-G-T

http://identifiers.org/hco/2/GRCh38#109348018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58820068-C-A

109348018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58820068-C-T

http://identifiers.org/hco/2/GRCh38#109348019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58820069-C-A

http://identifiers.org/hco/2/GRCh38#109348091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58820126-C-A

109348091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58820126-C-G

109348122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58820150-G-A

109349018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58821771-T-C

109349338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58822102-G-C

109349375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58822136-C-T

109349393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58822155-C-G

109349693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58822608-G-A

109349836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58822728-C-T

109350038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58822917-C-T

109350044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58822923-G-A

109350044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58822923-G-C

109350049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58822928-G-A

109350118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58823008-A-G

109354240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58827317-C-T

http://identifiers.org/hco/2/GRCh38#109354254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58827326-C-A

http://identifiers.org/hco/2/GRCh38#109354261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58827329-A-C

http://identifiers.org/hco/2/GRCh38#109354265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58827333-C-A

109354265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58827333-C-T

109354299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58827362-A-G

109354479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58827534-A-G

109355090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58827983-C-T

109355394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58828289-C-T

109355397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58828292-G-A

109355586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58828493-A-G

109355689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58828645-G-A

109355774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58828784-T-C

109355905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58829087-A-T

109355950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58829134-G-A

109356092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58829260-A-G

109356175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58829345-A-G

109356227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58829388-C-G

109356241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58829402-A-G

109356319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58829470-A-G

109356321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58829472-A-G

109356367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58829518-G-C

109356605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58829712-C-T

109356757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58829837-T-C

109356763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58829843-T-C

109356915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58829973-T-C

109357016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58830082-A-G

http://identifiers.org/hco/2/GRCh38#109370740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58842243-C-A

109370740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58842243-C-T

http://identifiers.org/hco/2/GRCh38#109371412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58842730-A-C

109371453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58842766-G-A

109371453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58842766-G-T

109371458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58842771-A-G

109371468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58842776-C-G

109371526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58842821-T-G

109371654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant
orthologous variants: 58842932-C-G

109371654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58842932-C-T

http://identifiers.org/hco/2/GRCh38#109371748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58843017-C-A

109371748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843017-C-G

109371748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843017-C-T

http://identifiers.org/hco/2/GRCh38#109371751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58843018-C-A

109371751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843018-C-G

109371751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843018-C-T

109371788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843054-T-A

109371815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843076-G-T

http://identifiers.org/hco/2/GRCh38#109371830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58843091-C-A

109371830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843091-C-G

109371838-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843100-C-G

109371848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843106-G-T

109371865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843117-C-G

http://identifiers.org/hco/2/GRCh38#109371868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58843120-C-A

109372058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843259-G-A

http://identifiers.org/hco/2/GRCh38#109372236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58843435-A-C

109372375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843535-T-A

109372375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843535-T-G

109372447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843582-G-A

109372623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58843720-A-G

http://identifiers.org/hco/2/GRCh38#109372764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58843834-A-C

109372999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58844020-C-T

109373010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58844031-C-G

109373086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58844098-C-T

109373241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58844264-G-A

109373256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58844279-A-G

109374622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58845139-G-C

109374672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58845198-A-G

http://identifiers.org/hco/2/GRCh38#109374805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58845323-A-C

109374805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58845323-A-G

109374805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58845323-A-T

109374946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58845454-G-A

109375024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58845529-C-T

109375089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58845587-A-G

109375249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58845724-G-A

109375249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58845724-G-C

109380491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58847889-C-T

http://identifiers.org/hco/2/GRCh38#109380720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58848064-C-A

109380720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58848064-C-T

109380809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58848150-C-T

109380819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58848157-T-C

109380928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58848269-G-A

109381153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58848480-C-T

109381237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58848553-G-A

109381255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58848571-G-A

http://identifiers.org/hco/2/GRCh38#109382599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58849150-C-A

109382748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58849275-C-T

109382753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58849280-G-A

109382822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58849323-A-T

109382827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58849328-T-C

109398393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58884835-G-A

109398542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58884994-A-G

http://identifiers.org/hco/2/GRCh38#109398585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58885038-C-A

109398595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 58885048-T-C

109398651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant
orthologous variants: 58885110-G-A

109398651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant
orthologous variants: 58885110-G-T

http://identifiers.org/hco/2/GRCh38#109398655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#58885114-C-A

109398681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant
orthologous variants: 58885140-G-T

109398703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58885162-A-G

109398704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant
orthologous variants: 58885163-A-G

109398751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58885210-T-C

109398796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58885255-G-A

http://identifiers.org/hco/2/GRCh38#109398844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58885303-C-A

109398844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58885303-C-G

http://identifiers.org/hco/2/GRCh38#109398959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58885417-C-A

109398959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58885417-C-T

109398986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58885443-G-T

http://identifiers.org/hco/2/GRCh38#109399043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58885502-C-A

109399043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58885502-C-T

http://identifiers.org/hco/2/GRCh38#109399049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58885508-A-C

109399049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58885508-A-T

109399050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58885509-G-A

109399050-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58885509-G-C

109399050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58885509-G-T

109399089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58885538-G-A

109399089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58885538-G-T

http://identifiers.org/hco/2/GRCh38#109399212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58885633-A-C

109399409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58885798-T-G

109399414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58885803-A-G

109399737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58885932-T-G

109399805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58885989-G-A

109399868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58886080-C-T

109399909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58886104-C-T

109399927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58886122-G-A

109399932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58886127-G-A

109399948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58886143-C-T

109400024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58886221-G-A

109400024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58886221-G-T

109404482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58890923-A-G

109404518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58890953-G-A

109404518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58890953-G-C

109404546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58890971-A-G

109404600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58891021-C-T

109404678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58891075-C-T

109404698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58891095-G-A

109404732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58891129-A-G

109404775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58891168-C-T

109404776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58891169-G-A

http://identifiers.org/hco/2/GRCh38#109404790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58891183-C-A

109404790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58891183-C-T

109404826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58891209-A-G

109405175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58891434-C-G

109405700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58891904-C-T

109405702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58891906-C-T

109405703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58891907-A-G

109405748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58891940-C-T

109405986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58892203-C-T

109406001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58892219-C-T

109406155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58892356-C-T

http://identifiers.org/hco/2/GRCh38#109406259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58892459-C-A

109406259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58892459-C-T

109406344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58894923-G-A

109406384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58894972-G-T

109406391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58894979-C-G

109406512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58895092-G-A

109406866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58895387-C-G

109406950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58895455-C-G

109407029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58895557-C-T

109407120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58895638-G-A

109407123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58895641-C-T

109407346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58895853-G-A

109407358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58895865-T-C

109407466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58895912-G-T

109407470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58895916-C-G

109407569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58896013-A-G

109407690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58896129-T-G

http://identifiers.org/hco/2/GRCh38#109407748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58896191-A-C

109407748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58896191-A-T

http://identifiers.org/hco/2/GRCh38#109410153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58897787-C-A

109410153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58897787-C-T

109410413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58898017-G-A

109410512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58898100-C-G

109410579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58898160-G-T

109410650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58898224-A-G

109410655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58898234-A-G

109410655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58898234-A-T

109410693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58898271-C-G

109410754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58898337-G-A

109410825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58898750-C-T

http://identifiers.org/hco/2/GRCh38#109410826-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58898751-A-C

109410831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58898756-G-C

109410831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58898756-G-T

109410861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58898786-G-A

109412270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58903783-C-G

http://identifiers.org/hco/2/GRCh38#109412373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58903889-C-A

109412373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58903889-C-T

109412402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58903919-A-G

109417402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58904564-G-T

109417416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58904577-G-C

109417621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58904747-C-T

109417636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58904762-G-A

109417658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58904784-T-G

109417738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58904866-G-A

109417837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58904947-G-T

109417852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58904962-G-A

109417954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58905053-A-G

109418084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58905179-C-T

109418225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58905288-G-A

109418322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58905394-G-T

109418426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58905479-C-T

109418432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58905485-C-G

109418452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58905504-G-T

109418507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58905561-A-G

109418510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58905564-C-G

109418530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58905583-C-T

109418706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58905688-G-C

109418713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58905695-C-T

109419339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58907552-G-T

109419408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58907624-A-T

109419454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58907672-G-A

109419454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58907672-G-T

109419475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58907694-T-C

http://identifiers.org/hco/2/GRCh38#109419522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58907741-C-A

109419522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58907741-C-T

109419554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant
orthologous variants: 58907770-G-A

109419554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant
orthologous variants: 58907770-G-T

109419898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58908079-A-G

109420223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58908887-C-G

http://identifiers.org/hco/2/GRCh38#109420224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58908888-C-A

109420224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58908888-C-T

109420356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58909014-G-A

109420904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58909218-C-T

109420910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58909239-A-G

109421277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58909867-G-C

109421368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58909954-G-A

109421705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58910228-G-A

109421791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58910311-C-T

109421876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58910390-T-C

109421896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58910410-A-G

109421914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58910428-C-T

109422132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58912404-G-C

http://identifiers.org/hco/2/GRCh38#109422210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58912478-A-C

109422210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58912478-A-G

109422246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58912504-T-C

109422281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58912540-G-A

109428604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58913106-C-T

109428705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58913184-A-G

109428777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58913241-A-T

109428841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58913338-G-A

109430242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58917047-G-C

109430247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58917052-C-T

109430297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58917102-C-T

109430667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58917841-G-A

http://identifiers.org/hco/2/GRCh38#109430701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58917877-C-A

109430704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58917880-T-C

109430707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58917883-T-C

109430750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58917928-C-T

109430753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58917931-G-C

109430758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58917936-G-T

109430994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918119-A-G

109431003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918128-G-A

109431024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918149-A-G

109431142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918246-G-C

http://identifiers.org/hco/2/GRCh38#109431199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58918300-C-A

109431251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918346-G-A

109431300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918399-A-G

109431405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918491-C-T

109431424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918510-T-C

109431497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918581-G-A

109431726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918661-G-A

109431835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918764-C-T

109431983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918827-C-T

http://identifiers.org/hco/2/GRCh38#109431984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58918828-C-A

109432000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918844-G-A

109432008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918852-A-G

109432063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918889-G-C

109432087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918906-T-G

109432101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918921-C-T

109432110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58918929-T-C

109432196-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58919009-C-G

109432379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58919156-T-C

109432405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58919181-G-T

109432411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58919187-C-T

109432492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58919261-T-G

109432493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58919262-G-A

109432493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58919262-G-C

109432493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 58919262-G-T

109432555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant
orthologous variants: 58919324-C-G

109432555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58919324-C-T

109432633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58919402-T-C

109432633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58919402-T-G

109432639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58919408-G-A

109432654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58919423-C-T

http://identifiers.org/hco/2/GRCh38#109432663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58919432-C-A

109432663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58919432-C-G

109432663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58919432-C-T

109432709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58919472-G-T

109432712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58919475-A-G

109432752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58919487-T-A

109432752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58919487-T-C

http://identifiers.org/hco/2/GRCh38#109432777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58919512-C-A

109432777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58919512-C-T

109432920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58919665-G-T

109433124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58919998-C-G

109433124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58919998-C-T

109433134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58920008-G-T

109433221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58920111-A-G

109433362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58920284-A-G

109433421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58920345-G-T

109433439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58920360-C-T

109433440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58920361-G-A

109433440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58920361-G-T

109433454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58920376-C-T

109435891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58920677-G-A

109436050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58920825-G-A

109436397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58921161-T-C

109436462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58921229-G-A

109436594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58921350-G-T

http://identifiers.org/hco/2/GRCh38#109436771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58922356-C-A

109436771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58922356-C-G

109436771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58922356-C-T

http://identifiers.org/hco/2/GRCh38#109436825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58922410-C-A

http://identifiers.org/hco/2/GRCh38#109437076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58922665-C-A

109437076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58922665-C-T

109437100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant
orthologous variants: 58922689-C-G

109437106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58922695-C-T

109437140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant
orthologous variants: 58922732-T-G

109437150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58922742-C-T

109437151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58922743-C-T

109437184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58922784-A-G

109437212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58922811-G-T

109437283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58922849-T-A

109437349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58922870-G-A

109437443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58922938-A-G

http://identifiers.org/hco/2/GRCh38#109437729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58923157-A-C

109437827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58923246-T-C

109437881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58923294-A-G

109438239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58923615-C-T

109438924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58926046-A-G

109438939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58926062-T-A

109438939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58926062-T-C

109439159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58926240-G-T

109439252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58926329-G-A

109439504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58926586-C-T

109440032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58927114-C-G

109440032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58927114-C-T

http://identifiers.org/hco/2/GRCh38#109440293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58927557-A-C

109440293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58927557-A-G

109440460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58927722-C-T

109440595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58927806-G-A

109440597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58927808-A-G

109440604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58927815-A-G

109440629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58927846-A-G

109440790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58927996-C-T

109440800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58928003-C-T

109441102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58928274-G-A

109441112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58928284-T-A

http://identifiers.org/hco/2/GRCh38#109441153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58928312-C-A

109441153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58928312-C-G

109449113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58939949-G-A

109449113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58939949-G-C

109449113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58939949-G-T

http://identifiers.org/hco/2/GRCh38#109449183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58940007-A-C

109449183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58940007-A-G

109449223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58940047-C-T

http://identifiers.org/hco/2/GRCh38#109449311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58940135-C-A

109449311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant
orthologous variants: 58940135-C-T

http://identifiers.org/hco/2/GRCh38#109449360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58940184-A-C

109449360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58940184-A-G

http://identifiers.org/hco/2/GRCh38#109449430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58940254-C-A

109449430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58940254-C-T

109449441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58940265-C-T

109449465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 58940289-A-G

109449528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58940352-C-T

109449620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58940429-A-T

109449689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58940511-T-G

109449772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58940602-T-A

109449918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58940760-G-T

109449942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58940784-A-G

109449981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58940833-C-T

109451376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58941649-G-C

109451466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58941721-T-G

109451467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58941722-C-T

109453927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58941895-G-A

http://identifiers.org/hco/2/GRCh38#109453941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58941907-C-A

109458331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58942971-T-C

109458542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58943152-G-A

109458603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58943236-T-A

109458603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58943236-T-C

109458603-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58943236-T-G

109458620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58943253-A-G

109458620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58943253-A-T

109458675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58943325-T-C

109459105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58943786-G-T

109459203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58943875-G-C

109459307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58943964-G-C

109459392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58944054-T-G

109459435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58944092-T-C

109459528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58944173-G-A

109459533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58944178-A-G

109459565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58944210-G-T

http://identifiers.org/hco/2/GRCh38#109459895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#58944454-A-C

109459904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58944463-G-A

109459925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24699
most severe consequence: intron variant
orthologous variants: 58944483-A-G