http://identifiers.org/hco/5/GRCh38#61332351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108026503-A-C

61332351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: missense variant
orthologous variants: 108026503-A-G

61332636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: missense variant
orthologous variants: 108026212-T-A

61332636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: missense variant
orthologous variants: 108026212-T-C

http://identifiers.org/hco/5/GRCh38#61333034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108025829-C-A

61333034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108025829-C-G

61333034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108025829-C-T

http://identifiers.org/hco/5/GRCh38#61333039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108025824-A-C

61333039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108025824-A-G

61333039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108025824-A-T

61333250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108025644-C-T

61333496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108025427-C-T

61333570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108025344-C-T

61333989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108025079-C-T

61334368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108024707-A-G

61334404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108024678-G-A

61334414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108024668-G-A

61334520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108024523-G-A

61334520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108024523-G-T

61334845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108024193-A-G

61334900-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108024139-T-A

61334909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108024130-C-G

61334909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108024130-C-T

61335321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108023706-C-G

61335743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108023292-T-C

61335831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108023194-T-C

61337974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108022297-G-T

61338175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108022055-T-G

61339866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108020203-G-A

61340035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108020035-T-C

61340257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108019823-T-C

61340768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108019101-C-T

61341866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108018632-C-G

61341866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108018632-C-T

61342255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108018553-A-G

61343022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108018048-C-T

61343264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108017796-T-C

61343754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108017043-A-G

61343971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108016827-C-T

61344320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108016493-G-T

61345193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108015752-A-G

61345444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108015331-C-G

61345548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108015219-T-C

61345748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108015042-C-T

61346099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108014786-C-T

61346298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108014601-G-A

http://identifiers.org/hco/5/GRCh38#61346377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108014483-A-C

61346453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108014365-T-C

61346560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108014260-C-T

61346921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108013816-T-C

61346921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108013816-T-G

http://identifiers.org/hco/5/GRCh38#61348829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108012302-C-A

61349034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108012113-T-C

61349279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108011926-C-G

61349328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108011882-G-C

61349745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108011569-G-C

61349897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108011319-A-G

http://identifiers.org/hco/5/GRCh38#61349913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108011306-A-C

61349913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108011306-A-G

61351675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108010913-C-T

61351802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108010833-T-C

61351974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108010590-C-T

http://identifiers.org/hco/5/GRCh38#61352096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108010485-C-A

61352096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108010485-C-G

61352096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108010485-C-T

61352450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108010190-T-C

61352575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108010087-C-T

http://identifiers.org/hco/5/GRCh38#61352662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108010006-C-A

61352909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108009798-T-G

61353327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108009388-T-A

61353327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108009388-T-G

61353411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108009315-C-T

61353665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108009138-T-C

61353760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108009038-T-A

61353888-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108008911-C-G

61355095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108007768-C-G

61355328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108007519-C-T

61355664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108007255-A-G

61357014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108006417-C-T

61357523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108006056-A-G

61357624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108005950-T-C

http://identifiers.org/hco/5/GRCh38#61357679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108005893-A-C

61357698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108005874-A-G

61357828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108005726-G-A

61359857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108005391-C-T

61359881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108005385-A-G

61360098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108005178-T-C

http://identifiers.org/hco/5/GRCh38#61360612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108004780-C-A

61360710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108004635-G-A

61360711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108004634-G-C

61360760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108004587-G-A

61360760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108004587-G-C

61360838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108004509-G-T

http://identifiers.org/hco/5/GRCh38#61361256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108004154-A-C

61361256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108004154-A-G

61362857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108002942-A-G

61363782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108002005-G-A

61364233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108001952-T-C

61364239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108001946-C-T

61364471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108001704-G-A

61364471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108001704-G-T

61364715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108001465-C-T

http://identifiers.org/hco/5/GRCh38#61364750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#108001432-A-C

61364964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108001246-T-C

61364983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108001227-T-G

61365627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108000874-G-T

61365758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108000739-G-A

61366344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108000437-C-T

61366377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108000406-A-G

61366723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 108000121-A-T

61367425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107999744-C-T

61367664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107999539-A-G

http://identifiers.org/hco/5/GRCh38#61367675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107999528-A-C

61370083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107997674-A-G

61370244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107997512-C-T

61370341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107997416-T-C

61370372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107997387-A-G

61370530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107997229-A-T

61370543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107997213-C-T

61370649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107997067-C-T

61370677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107997037-T-C

61370687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107996991-G-A

http://identifiers.org/hco/5/GRCh38#61370713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107996926-A-C

http://identifiers.org/hco/5/GRCh38#61370733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107996886-A-C

61371058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107996584-G-C

61371190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107994507-C-T

61371215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107994478-T-C

61371215-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107994478-T-G

61371258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107994436-A-G

http://identifiers.org/hco/5/GRCh38#61371369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107994324-C-A

61371447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107994247-T-C

61372011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107993684-G-A

61372076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107993643-A-T

61372120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107993586-T-C

61372138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107993571-G-A

61372249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107993388-A-G

61372361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107993277-T-C

61372371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107993267-G-T

61372412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107993233-T-C

61372429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107993216-G-C

61372633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107993005-A-G

61372797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107992840-C-T

61372838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107992807-T-A

61372838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107992807-T-G

61374132-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107989619-C-G

61374248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107989507-G-C

http://identifiers.org/hco/5/GRCh38#61374306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107989472-A-C

61374368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107989427-C-T

61374490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107989301-A-G

61379218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107988271-A-T

61379234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107988260-T-A

61379319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107988186-G-A

61379319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107988186-G-C

61379345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107988166-G-A

61379406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107988132-G-T

61379648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107987901-T-G

61379852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107987720-A-G

61379854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107987718-G-T

61379919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107987661-A-G

61379919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107987661-A-T

61379923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107987657-G-C

61380075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107987494-T-C

61380599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107987268-G-A

61380612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107987255-A-G

61380777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107986915-C-G

http://identifiers.org/hco/5/GRCh38#61380778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107986914-C-A

61381883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107986562-G-A

http://identifiers.org/hco/5/GRCh38#61381973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107986528-A-C

61382001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107986500-G-C

61382101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107986404-G-A

61382108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107986398-G-A

61382228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107986293-T-C

61382501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107986075-T-C

61382866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107986052-G-T

http://identifiers.org/hco/5/GRCh38#61382870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107986048-A-C

61382879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107986039-G-A

61382894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107986023-A-G

61382898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107986019-T-C

61382919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107985992-A-G

61383386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107985539-G-T

61383460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107985474-G-T

61384481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107985170-A-G

http://identifiers.org/hco/5/GRCh38#61384569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107985092-C-A

61384569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107985092-C-T

61384573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107985075-C-T

61384585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107985063-A-G

61384714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107984922-T-C

61385091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107984847-C-G

61385091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107984847-C-T

61385262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107984704-A-G

61385470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107984541-G-A

61385472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107984539-A-G

61385830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107984315-G-A

61385830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107984315-G-T

61385835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107984310-G-A

61385951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107984211-C-T

61386004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107984168-G-A

61386096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107984081-G-A

61386188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107984010-G-A

61386952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107983258-C-G

61386952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107983258-C-T

61386953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107983257-G-A

61388400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107982730-C-T

61388438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107982696-C-T

61389878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107982295-A-T

61389900-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107982269-T-G

61389913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107982256-A-T

61389935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107982234-G-C

61390015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107982156-T-G

61390207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107981999-C-G

61393772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107981230-A-G

61393991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107981036-T-C

61395609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107980167-A-G

61395609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107980167-A-T

61395774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107980008-A-G

http://identifiers.org/hco/5/GRCh38#61395965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107979854-A-C

61396695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107979200-T-G

61396788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107979136-C-T

61396892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107979058-G-C

61397106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107978859-A-G

61397111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107978854-G-A

61397197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107978762-C-T

61397225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107978738-A-G

61397396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107978592-G-A

61398486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107978163-T-C

61398653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107977996-A-G

61399291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107977623-T-C

61399418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107977530-A-G

61399427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107977521-C-G

61399550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107977408-C-T

61399734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107977235-A-G

61399855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107977135-C-T

61400233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107976838-A-G

61400303-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107976768-G-C

61401079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107974484-C-T

61403102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107972878-G-A

61403120-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107972860-G-C

61403306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107972707-T-C

61403361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107972629-A-G

61404410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107971779-G-A

61404924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107971369-T-C

61404992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107971304-A-G

61405751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107970628-T-G

61405789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107970592-A-G

61405843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107970539-T-C

61406126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107970278-A-G

61408884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron_variant, undefined
orthologous variants: 107967837-A-G

61408972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron_variant, undefined
orthologous variants: 107967752-G-T

61409046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107967685-G-C

61409046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107967685-G-T

61409064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107967663-G-A

61409818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107966985-G-A

61409873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107966928-G-A

61409873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107966928-G-T

61409931-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107966866-T-A

61410087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107966618-A-G

61416154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107965507-G-A

61416584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107964542-A-G

61416651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107964473-C-G

61417775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107964059-T-G

61417940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107963883-T-C

61417947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107963876-T-C

http://identifiers.org/hco/5/GRCh38#61417955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107963868-A-C

61417955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107963868-A-G

61418215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107963606-T-C

61419162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107963327-A-G

http://identifiers.org/hco/5/GRCh38#61419311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107963173-A-C

61419347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107963138-T-G

61419466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107963006-C-G

61419871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107962630-T-C

61424438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107962205-G-T

61424461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107962182-G-A

61424640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107961841-C-T

61428033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107960301-A-G

61428210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107960130-A-G

61429453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107958551-A-G

61429466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107958538-G-A

61429536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107958478-C-G

61429871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107958170-A-G

61430006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107958124-A-G

61430007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107958123-G-A

61430148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107957999-T-G

61430200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107957947-G-T

61430226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107957919-C-T

61430792-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107956561-T-A

61430915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107956469-T-A

61430941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107956444-G-A

61430983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107956400-G-A

61431903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107956161-T-A

61431903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107956161-T-C

61431904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107956160-T-C

61432154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107955939-T-C

61432340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107955759-A-T

61432373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107955729-A-G

61432437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107955622-A-G

61432437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107955622-A-T

61432487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107955568-C-T

61433213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107954688-G-A

61433307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107954598-A-G

61435003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107954025-C-T

61435034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107953991-C-T

61435164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107953868-A-G

61435196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107953836-G-A

61435264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107953765-C-T

http://identifiers.org/hco/5/GRCh38#61436256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107952544-C-A

61436256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107952544-C-T

61436310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107952492-C-G

61437073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107951984-C-T

61437250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107951763-A-G

61437407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107951615-G-A

61437454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107951569-G-A

61437693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107951400-G-A

61437715-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107951384-T-A

61437715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107951384-T-C

61438643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107950296-T-C

61438765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107950177-G-A

61439301-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107949675-T-A

http://identifiers.org/hco/5/GRCh38#61439307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107949669-C-A

61439343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107949632-A-G

61439476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107949513-A-G

61439608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107949398-C-T

61440109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107948900-G-A

61440716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107948334-G-A

61440738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107948312-T-C

61441087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107948005-G-A

61450655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107947648-A-G

61450795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107947526-G-A

61450954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron_variant, undefined
orthologous variants: 107947379-G-T

61451080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron_variant, undefined
orthologous variants: 107947250-A-G

61451115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron_variant, undefined
orthologous variants: 107947215-T-A

61451124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron_variant, undefined
orthologous variants: 107947206-C-T

61454892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107945711-T-G

http://identifiers.org/hco/5/GRCh38#61454991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107945640-C-A

61455339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107945284-A-G

61455375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107945247-T-G

61455393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107945229-A-G

61455529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107945084-C-T

http://identifiers.org/hco/5/GRCh38#61455800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107944850-C-A

http://identifiers.org/hco/5/GRCh38#61455809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107944811-C-A

61455809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107944811-C-G

61456370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107943986-A-G

61456503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107943911-C-T

61456753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107943686-G-A

61456811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107943633-A-G

61456812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107943632-T-C

61459102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107941774-T-A

61459153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107941764-T-C

61459518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107941429-G-A

61459518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107941429-G-T

61459539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107941408-C-G

61459579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107941367-T-G

61459682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107941217-A-G

61459763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107940854-T-A

61459772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107940845-A-G

61460081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107940510-G-A

61460234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107940410-T-C

61460374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107940258-G-T

61460506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107940118-G-A

61461261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107939436-G-T

61461438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107939288-T-A

61461518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107939211-C-G

61461552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107939177-G-A

61461725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107939026-A-G

http://identifiers.org/hco/5/GRCh38#61461731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107939020-A-C

61461731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107939020-A-G

61461983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107938814-T-A

61461989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107938808-A-G

61462259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107938559-A-T

http://identifiers.org/hco/5/GRCh38#61462478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107938351-C-A

61462857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107937963-C-T

61462912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107937919-C-T

61463048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107937793-G-T

61463346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107937404-C-T

61463350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107937400-A-G

61463410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107937341-G-C

61463411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107937340-T-C

61463559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107937180-G-A

61463562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107937177-C-G

61463562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107937177-C-T

61464668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107936231-T-C

61465009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107935922-G-A

61465023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107935908-G-T

61465039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107935894-G-A

61465101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107935841-C-G

61465416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107935630-T-C

61465444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107935602-A-G

http://identifiers.org/hco/5/GRCh38#61465446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107935600-A-C

61465807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107935248-T-C

61465807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107935248-T-G

61466194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107934844-G-T

61466213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107934822-T-G

http://identifiers.org/hco/5/GRCh38#61466234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107934801-C-A

61466234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107934801-C-T

61466305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107934735-C-T

61466494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107934497-A-G

61467252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107932963-A-T

61467369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107932844-C-T

61467530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107932739-T-A

61467530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107932739-T-C

61467935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107932370-T-A

61468076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107932234-T-C

61468159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107932152-G-A

61468463-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107927830-A-T

61468567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107927767-C-T

61468580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107927757-G-A

61468585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107927752-T-A

61468662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 107927676-G-C

61468718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107927600-G-A

http://identifiers.org/hco/5/GRCh38#61468802-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107927523-A-C

61468843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107927484-T-C

61468843-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107927484-T-G

61468866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107927461-A-G

61468881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107927450-G-A

61469042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107927311-A-G

61469213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107927231-T-C

61469332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107927165-T-C

61469444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107927071-T-A

http://identifiers.org/hco/5/GRCh38#61469666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107926867-C-A

61469706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107926837-A-G

61469706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107926837-A-T

61469716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107926827-T-C

61470226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107926491-T-C

61470491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107926245-G-T

http://identifiers.org/hco/5/GRCh38#61470730-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107925842-A-C

61470777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107925801-G-A

61470970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107925664-G-C

61471310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107925451-G-A

61471435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107925329-T-C

61471577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107925199-G-T

http://identifiers.org/hco/5/GRCh38#61472257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107924879-A-C

61472393-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107924768-T-A

61472419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107924742-G-A

http://identifiers.org/hco/5/GRCh38#61473138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107924096-A-C

61473138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107924096-A-T

61473173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107924068-T-A

61473785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107923034-G-A

61474401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107922514-T-G

61475092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107921488-C-G

http://identifiers.org/hco/5/GRCh38#61475093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107921487-A-C

61475378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107921003-T-G

61475426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107920972-A-G

61475807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107920577-T-C

61475894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107920495-G-A

61476396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107920331-G-A

61476396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107920331-G-T

61477010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107919575-G-A

61477239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107919282-A-G

61477394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107919151-G-A

61477394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107919151-G-T

61477402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107919145-C-T

61477691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107918798-C-G

61477720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107918768-T-C

61477975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107918493-G-A

61477975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107918493-G-C

61478030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107918437-A-G

61478197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107918282-C-G

61478526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107918034-T-C

61478811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107917752-C-T

61478850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107917718-T-G

61479246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107917625-A-T

61479526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107917304-C-G

61479814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107917043-G-A

61480453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107916301-C-G

61480550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107916216-T-A

61480550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107916216-T-C

61481081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107915704-T-A

61481254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107915501-C-T

61481349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107915413-C-T

61481482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107915291-C-T

61481564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107915213-T-G

61481635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107915181-T-C

61481986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107914852-A-G

61482034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107914806-G-A

61482222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107914614-G-A

61482734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107914259-A-G

61482755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107914236-C-T

61482766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107914225-G-C

61484181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107913579-T-C

61490682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107910175-A-G

61490682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107910175-A-T

http://identifiers.org/hco/5/GRCh38#61490989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107909852-A-C

61490989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107909852-A-G

61491005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107909836-G-A

61491064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107909794-A-G

61491163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107909700-A-G

61491548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107909297-T-G

61491873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107908661-G-C

61491961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107908595-A-G

61492051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107908517-G-A

61492588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107907978-T-C

61492713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107907884-C-T

61492766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107907832-A-T

61493035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107907550-G-T

61493053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107907532-C-T

http://identifiers.org/hco/5/GRCh38#61493347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107906966-C-A

61493570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107906802-C-T

61493652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107906717-T-C

61493998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107906420-A-G

61494242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107906260-T-G

61494462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107906043-A-G

http://identifiers.org/hco/5/GRCh38#61494533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107905978-C-A

61494533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107905978-C-T

61494684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107905849-A-G

61494910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107905645-A-G

61495295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107905348-A-G

61495597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107905039-C-T

61495703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107904940-G-T

61495908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107904747-T-C

61496336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107904249-G-T

61496378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107904207-A-G

61497137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107903445-G-C

61497186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107903402-T-C

61497406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107903183-T-C

61497501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107903106-C-T

61497513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107903094-A-G

61497770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107902828-C-T

61497836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107902762-C-T

61497994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107902606-C-G

61497994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107902606-C-T

61498113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107902485-G-A

61498652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901977-C-G

61498652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901977-C-T

61498678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901938-A-G

61498679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901937-T-C

61498724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901893-A-T

61499211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901501-T-C

61499321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901410-G-T

61499392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901362-T-C

61499454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901301-G-A

61499455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901300-G-A

61499455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901300-G-C

61499568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901225-G-A

61499609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901183-T-C

61499757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901047-A-G

61499757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107901047-A-T

http://identifiers.org/hco/5/GRCh38#61500610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107900591-C-A

61500610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107900591-C-T

61501679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107899688-A-T

http://identifiers.org/hco/5/GRCh38#61501866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107899537-A-C

61502138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107899101-T-G

61502271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107898964-G-A

61502293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107898942-G-A

61502479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107898775-A-G

http://identifiers.org/hco/5/GRCh38#61502501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107898754-A-C

61503620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107898057-A-G

61503628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107898049-T-C

61503727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107897904-T-C

61503894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107897743-T-C

61504035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107897609-C-T

61504155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107897499-A-G

61504845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107896809-G-C

61504864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107896780-G-A

61505075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107896565-T-C

61505238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107896431-C-G

61505341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107896324-T-G

61505368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107896297-C-G

http://identifiers.org/hco/5/GRCh38#61506216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107895959-A-C

http://identifiers.org/hco/5/GRCh38#61506884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107895604-C-A

61506979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107895506-C-T

61507040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107895446-T-C

61507042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107895444-A-G

61507098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107895387-C-T

61507168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107895322-G-A

http://identifiers.org/hco/5/GRCh38#61507374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107895140-A-C

61507374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107895140-A-G

61507565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107894925-G-A

61507681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107894814-G-C

61507686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107894812-A-G

61507830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107894452-G-A

61507830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107894452-G-T

61508008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107894287-A-G

61508353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107893925-A-G

61508425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107893852-T-A

61510135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107893395-A-G

61510167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107893363-A-G

61510521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107893031-G-T

61510665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107891046-T-A

61510799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107890916-G-A

61510887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107890822-G-C

61511100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107890614-G-A

61511355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107890370-T-C

61511914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107889866-A-G

http://identifiers.org/hco/5/GRCh38#61512541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107889505-A-C

61512629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107889433-T-G

61512928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107889211-C-G

61512928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107889211-C-T

61513007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107889117-G-A

61513147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107888976-T-A

61513469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107888720-T-A

61519230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107886504-C-T

61519441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107886346-G-A

61519480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107886302-T-C

61519622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107886168-G-A

61519623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107886167-T-C

61520165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107885981-C-T

61520281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107885865-T-A

61520305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107885845-G-C

61520655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107885382-C-T

61520678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107885359-T-G

61520802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107885238-T-C

61520822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107885218-G-A

61520997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107885054-G-T

61521257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 107884902-A-G

61521433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 107884726-G-A

61521433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 107884726-G-T

61521475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107884685-A-G

61521476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107884684-G-A

61521554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107884638-T-A

61521554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107884638-T-G

61521762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107884453-G-A

61522008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107884239-C-T

61522167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107884156-C-G

61522210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107884110-C-T

61522296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107884039-G-T

61522416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107883926-C-G

61522764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107883622-A-G

61522937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107883478-C-T

61522950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107883465-T-C

http://identifiers.org/hco/5/GRCh38#61523280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107882933-A-C

61523328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107882899-A-G

61523447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107882789-G-A

61523523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107882729-G-A

61523523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107882729-G-C

61523621-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107882664-A-T

61523629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107882652-T-A

61523889-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107882496-T-A

61523901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107882487-A-T

61524004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107882385-T-C

61524299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107882100-A-G

http://identifiers.org/hco/5/GRCh38#61524344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107882055-C-A

61524344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107882055-C-T

61524556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107881865-C-G

61524705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107881721-G-A

61524705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107881721-G-T

61524907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107881560-G-C

61524967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107881511-T-G

61525135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 107881343-C-T

61525617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107880853-C-T

61525680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107880786-A-G

61525680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107880786-A-T

61525685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107880781-G-A

61525690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107880776-G-A

61525690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107880776-G-T

61525697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107880769-G-A

61526073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107880397-A-G

61526102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107880368-G-A

61526420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107880047-C-T

61526432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107880035-A-G

61526488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107879975-T-C

61526496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107879967-T-C

61526607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107879818-C-T

61526780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107879631-C-G

61526803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107879608-C-T

61526842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107879569-A-G

61526919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107879499-G-A

61527322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107878801-T-C

61527448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107878680-A-G

61527489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107878589-T-A

61527521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107878559-T-A

61527521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107878559-T-C

61527731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107878371-A-G

61527794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107878284-A-G

61528038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107878096-A-T

61528158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107878004-G-A

61528195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107877973-G-T

61528949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107877606-T-C

61529042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107877524-A-T

61529046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107877520-G-A

61529307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107877443-T-A

61529396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107877355-A-G

61529999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107876941-T-C

61530205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 107876759-C-T

http://identifiers.org/hco/5/GRCh38#61530279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107876684-A-C

61530279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107876684-A-G

61530284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107876472-T-A

61530296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107876460-G-T

61530327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107876425-G-A

61530327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107876425-G-T

61530391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107876370-T-C

61530715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107876083-T-C

61530882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107875917-G-A

61530882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107875917-G-T

61531055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107875781-T-C

61531142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107875599-A-G

61531375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107875245-G-A

61531375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107875245-G-T

61531732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 107874898-T-A

http://identifiers.org/hco/5/GRCh38#61531811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107874839-C-A

61531811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107874839-C-T

61531881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107874785-T-C

61531903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107874762-A-G

61531923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107874744-C-T

61532711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107874044-T-C

61532846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107873888-C-T

61533111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107873599-G-A

61533124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107873586-A-G

61533148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107873554-C-G

61533161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107873541-T-C

61533165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107873537-T-C

61533217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107873489-A-G

61533580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107873150-G-A

61533580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107873150-G-C

61533721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107873031-C-G

61534035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107871890-T-C

61534145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107871797-A-G

61534210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107871743-T-G

61534304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107871632-A-T

61534660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107871261-G-A

61534734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107871199-A-G

61534747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107871186-A-G

61534747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107871186-A-T

61534882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107871053-G-A

61534882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107871053-G-T

61534998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107870954-C-G

61535052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107870913-G-A

61535052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107870913-G-T

61535131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107870825-T-C

61535320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107870644-T-C

61535436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107870514-T-C

61535460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107870490-A-G

61535635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107870316-C-T

61535636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107870315-C-T

61535708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107870240-T-C

61536062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107870014-C-G

61536070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107870005-G-A

61536070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107870005-G-T

61536282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107869836-T-G

61536543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107869567-T-C

http://identifiers.org/hco/5/GRCh38#61536705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107869325-A-C

61536932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107869105-A-G

61537167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107868870-G-A

61537259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107868841-G-T

61537425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107868699-T-A

61537430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107868697-C-T

61537488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107868641-A-G

http://identifiers.org/hco/5/GRCh38#61537643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107868491-C-A

61537666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107868468-G-A

61537666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107868468-G-T

61537878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107868289-T-C

61538440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867994-A-G

61538475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867959-G-C

61538475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867959-G-T

61538680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867854-G-T

61538692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867845-G-T

http://identifiers.org/hco/5/GRCh38#61538804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107867749-C-A

61538804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867749-C-T

61538989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867564-G-A

61538989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867564-G-T

http://identifiers.org/hco/5/GRCh38#61538991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107867562-C-A

61538991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867562-C-T

61538996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867551-T-A

61538996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867551-T-C

61539008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867538-T-C

61539014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867532-G-A

61539018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867519-G-A

61539018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867519-G-T

61539103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867439-A-G

61539103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867439-A-T

61539106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867436-T-A

http://identifiers.org/hco/5/GRCh38#61539120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107867411-A-C

http://identifiers.org/hco/5/GRCh38#61539257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107867268-C-A

61539301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867225-T-C

61539322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867199-C-T

61539478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867029-T-C

61539478-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867029-T-G

61539494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107867017-T-C

61539865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107866676-T-G

61539945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107866592-T-C

61539945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107866592-T-G

61540368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107866197-G-A

61541381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865627-C-T

http://identifiers.org/hco/5/GRCh38#61541396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107865613-A-C

61541396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865613-A-T

61541512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865520-A-G

61541704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865335-C-T

61541753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865311-C-G

61541753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865311-C-T

61541768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865292-A-G

61541776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865284-G-T

http://identifiers.org/hco/5/GRCh38#61541825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107865244-C-A

61541825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865244-C-G

61541825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865244-C-T

61541866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865204-G-A

61541866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865204-G-T

61542005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865080-A-G

61542005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865080-A-T

61542098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865020-C-T

61542103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107865015-T-A

61542207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron variant
orthologous variants: 107864934-A-G

61542290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron_variant, missense_variant, splice_region_variant
orthologous variants: 107864879-G-T

61542317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: intron_variant, missense_variant
orthologous variants: 107864868-G-A

61542511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107864709-G-A

61542511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107864709-G-C

61542575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107864657-C-T

61542843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107864440-C-T

61542916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107864403-T-C

61543137-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107864146-G-C

61543137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107864146-G-T

61543191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107864092-G-A

61543271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107864012-T-G

61543318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107863966-T-C

http://identifiers.org/hco/5/GRCh38#61543325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107863960-C-A

61543325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107863960-C-T

61543401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107863886-G-A

61543401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107863886-G-T

http://identifiers.org/hco/5/GRCh38#61543407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#107863881-C-A

61543407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 107863881-C-T

61543529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 107863756-G-A

61544108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 107863177-G-A

61544108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 107863177-G-C

61544246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 107863039-A-G

61544357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3 prime UTR variant
orthologous variants: 107862930-G-A

61544357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3 prime UTR variant
orthologous variants: 107862930-G-C

61544357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3 prime UTR variant
orthologous variants: 107862930-G-T

61545121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29316
most severe consequence: 3 prime UTR variant
orthologous variants: 107862162-G-A