130014183-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26255688-A-T

130014208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26255663-A-G

130014346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26255461-T-C

130014579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26255229-G-A

130014615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26255195-T-A

130014615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26255195-T-C

130015641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26254847-G-T

130016084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26254470-G-A

130016266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5 prime UTR variant
orthologous variants: 26254305-C-T

http://identifiers.org/hco/6/GRCh38#130017149-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26253417-A-C

130017351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26253216-T-C

130017893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26252668-C-T

130018143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26252434-C-G

130018143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26252434-C-T

http://identifiers.org/hco/6/GRCh38#130018440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#26252128-C-A

130018440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 26252128-C-G

130018440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 26252128-C-T

130018518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5 prime UTR variant
orthologous variants: 26252050-G-A

130018518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5 prime UTR variant
orthologous variants: 26252050-G-T

130018747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, undefined
orthologous variants: 26251820-G-A

130018747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, undefined
orthologous variants: 26251820-G-T

130019051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26251512-G-A

130019102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26251462-G-A

130019103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26251461-T-C

130019330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26251203-C-G

130019433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26251075-G-A

130019433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26251075-G-C

130019443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26251065-G-A

130019443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26251065-G-T

http://identifiers.org/hco/6/GRCh38#130019581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26250920-C-A

130019581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26250920-C-T

130020262-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26250124-G-T

130020393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26250008-G-A

130020393-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26250008-G-C

130020393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26250008-G-T

130020397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26250004-G-A

130020397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26250004-G-C

130020397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26250004-G-T

http://identifiers.org/hco/6/GRCh38#130020474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26249886-C-A

130020474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26249886-C-T

130020541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26249819-T-C

130020770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26249564-G-A

130020787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26249547-G-A

130020787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26249547-G-T

130021078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26249235-G-C

130021289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26249032-C-T

http://identifiers.org/hco/6/GRCh38#130021545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26248786-C-A

130021980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 26248324-C-T

130021996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26248312-G-A

http://identifiers.org/hco/6/GRCh38#130022094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26248130-C-A

130022094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 26248130-C-G

130022188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26248037-G-T

130022408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26247857-A-G

http://identifiers.org/hco/6/GRCh38#130022585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26247042-A-C

130022701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26246929-C-G

130022798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26246823-G-C

130022941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26246698-A-G

130023037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26246617-C-T

130023410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26246006-G-A

130023422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26245994-A-G

130023439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26245991-A-G

130023633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26245816-C-T

130024007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26244997-T-A

130024082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26244922-A-G

130024275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26244724-G-A

130024328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26244675-C-G

130024427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26244572-A-G

130024431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26244568-A-G

130024457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26244542-A-G

130026092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26243134-G-A

130026092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26243134-G-T

130026377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26242859-G-A

130026683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26242166-A-G

130026834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26242048-T-C

130027146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26241537-C-T

130027263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26241433-A-T

http://identifiers.org/hco/6/GRCh38#130027331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26241361-A-C

130027681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26240994-T-C

130027732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26240947-T-G

130027859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26240810-C-T

http://identifiers.org/hco/6/GRCh38#130028036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26240626-C-A

130028437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26240250-C-G

130033512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26235888-G-T

130034135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26234877-C-T

130034340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26234732-T-C

130034598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, undefined
orthologous variants: 26234485-A-G

130034648-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26234435-T-G

130034740-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, undefined
orthologous variants: 26234330-G-C

130035342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26233086-A-G

130035505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, undefined
orthologous variants: 26232854-G-T

130036157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26232300-G-C

130036372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26232113-A-G

130036388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26232098-A-G

130036461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26232025-T-C

130042542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26228390-A-G

http://identifiers.org/hco/6/GRCh38#130042612-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26228332-A-C

http://identifiers.org/hco/6/GRCh38#130042842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26228114-C-A

130042842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26228114-C-T

130042949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26227933-T-G

130043029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26227857-T-A

130043076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26227811-T-C

130043189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26227711-A-G

130043197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26227703-G-T

130043224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26227676-A-G

http://identifiers.org/hco/6/GRCh38#130043429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26227331-C-A

130043513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26227238-C-G

130043663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26227080-G-A

130043663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26227080-G-C

130043744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26227004-G-A

130043744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26227004-G-T

130044185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26226059-A-G

130045480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26224399-T-A

130045704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26224243-A-G

130045787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26224164-T-C

130045986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26223993-C-T

130046034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26223934-G-A

130046252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26223466-A-G

130046283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26223443-A-G

130046379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26223351-C-T

130046394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26223315-C-T

130046508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26223198-G-T

130046563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26223141-A-G

130046851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26222764-C-T

130046976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26222684-T-G

130047136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26222537-A-G

http://identifiers.org/hco/6/GRCh38#130047148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26222525-C-A

130047148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26222525-C-T

http://identifiers.org/hco/6/GRCh38#130047266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26222426-A-C

130047498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26222212-G-A

130047851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26221897-A-G

130048047-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26221714-A-T

http://identifiers.org/hco/6/GRCh38#130048511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26221491-A-C

130048662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26221329-A-G

130048662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26221329-A-T

130048860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26221160-T-C

130048863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26221157-G-A

130049109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26220793-T-C

http://identifiers.org/hco/6/GRCh38#130049194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26220709-C-A

130049194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26220709-C-G

130049194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26220709-C-T

130049200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26220703-G-C

130049240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26220658-G-A

130049240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26220658-G-C

130049240-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26220658-G-T

130049251-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26220647-A-T

130049351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense variant
orthologous variants: 26220550-G-A

130049399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26220502-G-A

130049503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26220409-G-T

130049592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26220317-T-A

130049592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26220317-T-C

http://identifiers.org/hco/6/GRCh38#130049657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26220245-C-A

130049657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, missense_variant
orthologous variants: 26220245-C-G

130049657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, missense_variant
orthologous variants: 26220245-C-T

http://identifiers.org/hco/6/GRCh38#130049720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26220179-C-A

http://identifiers.org/hco/6/GRCh38#130049894-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26220010-A-C

130049898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26220006-T-C

130050246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26219664-A-G

130050258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26219652-T-C

130050338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26219561-A-G

130050480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26219394-T-C

130050561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26219314-C-T

130050704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26219172-A-G

130050887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26219014-A-G

130050892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26219009-A-T

130050958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26218951-C-T

130051020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26218850-G-A

130051062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26218744-G-C

130051109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26218696-A-G

130051181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26218624-A-T

130051218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26218593-G-A

130051218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26218593-G-T

http://identifiers.org/hco/6/GRCh38#130051507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26218311-C-A

130051510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26218308-T-A

130051518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26218300-T-C

130051559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26218261-A-T

130051694-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26218147-T-G

http://identifiers.org/hco/6/GRCh38#130051844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26217996-A-C

130051998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26217890-G-A

130052020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26217868-G-A

130052020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26217868-G-T

130052678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26217113-A-G

130052753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26217041-C-T

130052776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26217019-A-G

130052776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26217019-A-T

http://identifiers.org/hco/6/GRCh38#130052787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26217008-A-C

130052788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26217007-T-C

130052882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense variant
orthologous variants: 26216913-T-G

130053098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26216693-A-G

130053098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26216693-A-T

130053881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26216645-A-G

130054218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26216350-A-T

130054350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26216245-C-G

130054368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26216226-A-G

130054430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26216152-A-G

130054506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26216077-A-G

130054508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26216075-G-A

130054575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26215997-C-T

130054679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26215908-A-G

130054713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26215877-C-T

130054719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26215871-C-T

http://identifiers.org/hco/6/GRCh38#130054781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26215756-C-A

130054914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26215434-G-A

http://identifiers.org/hco/6/GRCh38#130054934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26215416-C-A

130054934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26215416-C-G

130054934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26215416-C-T

130054979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26215385-A-G

130054979-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26215385-A-T

130055023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26215344-G-T

130055085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26215285-A-G

130055140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26215230-T-C

130055141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26215229-T-C

http://identifiers.org/hco/6/GRCh38#130055161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26215209-C-A

130055161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26215209-C-G

130055324-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26215055-T-A

130055329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26215050-G-A

130055329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26215050-G-T

130055744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26214869-C-T

130055789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26214841-A-G

http://identifiers.org/hco/6/GRCh38#130057096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26213996-C-A

130057274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213879-G-A

130057274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213879-G-C

130057274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213879-G-T

130057365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213793-G-C

130057365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213793-G-T

http://identifiers.org/hco/6/GRCh38#130057381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26213777-C-A

130057435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26213726-T-G

http://identifiers.org/hco/6/GRCh38#130057510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26213651-C-A

130057510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213651-C-T

http://identifiers.org/hco/6/GRCh38#130057535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26213627-A-C

130057535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213627-A-G

130057538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213624-A-G

http://identifiers.org/hco/6/GRCh38#130057606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26213552-C-A

130057627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213534-T-C

130057674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213487-C-T

130057693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213482-G-T

130057711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213464-G-A

130057739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213432-G-A

130057854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213347-G-A

130058300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26213253-A-G

130060188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26212078-G-A

130060188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26212078-G-T

130060210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26212056-T-A

130060210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26212056-T-C

130060210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26212056-T-G

http://identifiers.org/hco/6/GRCh38#130060236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26212024-C-A

130060236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26212024-C-G

130060236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26212024-C-T

130060262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26211993-T-C

http://identifiers.org/hco/6/GRCh38#130060263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26211992-A-C

130060263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26211992-A-T

130060702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26211728-A-T

http://identifiers.org/hco/6/GRCh38#130060731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26211705-C-A

130060754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26211682-A-T

130064870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26208929-T-C

130064872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26208927-A-G

130064897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26208906-G-C

130064947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26208862-C-T

130065085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26208747-C-G

130065199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26208641-C-G

130065364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26208498-A-G

130065503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26208345-A-G

130065546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26208306-C-T

130066332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26207871-A-G

130066526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26207678-A-G

http://identifiers.org/hco/6/GRCh38#130066546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26207658-C-A

130066546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26207658-C-T

130066551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26207653-T-G

130066765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26207453-A-G

130068151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26206306-C-T

130068434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26206058-G-A

130068435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26206057-A-T

130068466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26206027-T-C

130068492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26205999-A-G

130068504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26205987-G-C

130068504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26205987-G-T

130068521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26205970-A-G

130068532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26205959-A-T

130068697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26205798-T-C

http://identifiers.org/hco/6/GRCh38#130069144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26205369-A-C

130069165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26205368-T-C

130069598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26205000-C-T

130069635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26204964-A-G

130069676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26204925-C-T

130069723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26204892-C-G

130069723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26204892-C-T

130070335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26204346-A-G

130070379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26204302-T-A

130070644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26204042-G-A

130070646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26204040-A-G

http://identifiers.org/hco/6/GRCh38#130070736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26203949-A-C

130070736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26203949-A-T

130070841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26203865-A-G

130070841-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26203865-A-T

130070851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26203854-G-A

130070851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26203854-G-T

130070896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 26203809-G-A

130070988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26203722-T-C

130071195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26203502-T-A

130071227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26203170-G-T

130071250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26203147-T-A

130073948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26202193-G-T

130074435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26201803-T-C

130074455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26201783-A-T

130074544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26201103-T-C

130074588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26201047-G-A

130074628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26201004-C-G

130074686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26200943-C-T

130074760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26200865-A-G

130074844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26200779-G-A

130074844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26200779-G-C

130075073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26200567-A-G

130075084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26200556-G-T

130075212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26200435-G-A

130075465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26200231-A-G

130075762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26199978-A-G

130075762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26199978-A-T

130076367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26199759-C-G

130076472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26199661-T-C

130076633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26199532-G-A

130076752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26199457-T-C

130076796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26199409-G-C

130076923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26199291-A-G

130077033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26199195-T-C

130077052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26199176-G-A

130077061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26199167-A-G

130077124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26199116-A-G

130077525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26198321-G-C

130077587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26198262-G-A

130077587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26198262-G-C

http://identifiers.org/hco/6/GRCh38#130077708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26198156-C-A

130078075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26195149-T-C

130078282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26194646-C-T

130078477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26194431-A-T

http://identifiers.org/hco/6/GRCh38#130078532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26194375-A-C

130078532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26194375-A-G

130078532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26194375-A-T

130078574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26194333-C-T

http://identifiers.org/hco/6/GRCh38#130078676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26194205-C-A

130078691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26194188-T-C

http://identifiers.org/hco/6/GRCh38#130078702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26194145-A-C

130078702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26194145-A-G

130078722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26194131-T-C

130078728-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26194125-T-A

http://identifiers.org/hco/6/GRCh38#130078735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26194117-C-A

130078768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26194085-G-T

130078883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26193979-G-A

130079024-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26193855-G-C

130081229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26193656-A-G

130081877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26193350-C-T

130081922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26193304-C-T

130082171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26192970-G-A

130082694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26192245-A-G

130082694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26192245-A-T

http://identifiers.org/hco/6/GRCh38#130082875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26192040-A-C

130082906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26192008-G-T

130083477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191623-G-A

130083477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191623-G-T

130083487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191613-T-G

130083490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191610-G-C

130083490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191610-G-T

130083576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191519-T-C

http://identifiers.org/hco/6/GRCh38#130083615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26191478-C-A

130083615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 26191478-C-T

http://identifiers.org/hco/6/GRCh38#130083625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26191468-C-A

130083673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26191420-T-C

130083682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26191411-G-A

130083709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191384-A-G

http://identifiers.org/hco/6/GRCh38#130083717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26191376-C-A

130083717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191376-C-T

130083763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191317-A-G

130083820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26191275-A-T

130085340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26190217-A-T

130085403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26190165-T-C

130085454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26190118-A-G

http://identifiers.org/hco/6/GRCh38#130086121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26189873-A-C

130086295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26189700-A-G

http://identifiers.org/hco/6/GRCh38#130086322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26189673-A-C

130086322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26189673-A-T

http://identifiers.org/hco/6/GRCh38#130086323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26189672-C-A

130086323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26189672-C-G

130086325-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26189670-T-A

130086325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26189670-T-C

http://identifiers.org/hco/6/GRCh38#130086339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26189656-C-A

130086339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26189656-C-T

130086344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26189649-A-T

130086409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26189588-A-G

130086478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26189516-A-G

130086478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26189516-A-T

130086538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26189461-A-G

130086650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26189243-G-A

130086723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26189169-T-G

130086918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26188931-T-C

130086922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26188928-A-G

130086938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26188912-A-G

130087051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26188789-G-C

130087093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26188748-T-C

130087361-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26188094-T-G

http://identifiers.org/hco/6/GRCh38#130087363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26188092-A-C

130087366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26188089-C-T

130087570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26187892-T-C

130087677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26187781-A-G

130087776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26187687-T-C

130087956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26187519-T-C

130087982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26187504-T-G

130088022-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26187491-T-A

130088393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26187126-A-G

130091415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26180776-G-A

130092226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26180126-G-A

130092374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26180008-T-A

130092374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26180008-T-G

130092418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26179966-A-G

http://identifiers.org/hco/6/GRCh38#130092610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26179781-A-C

130092610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26179781-A-G

130092621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26179770-T-G

130092688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26179690-T-C

130092688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26179690-T-G

http://identifiers.org/hco/6/GRCh38#130092720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26179651-C-A

130092720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26179651-C-T

130092793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense variant
orthologous variants: 26179585-G-C

130092909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26179469-A-G

130092909-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26179469-A-T

130092987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26179392-C-T

130093984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26178953-G-A

130094033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26178915-T-C

130094158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26178785-G-T

130094169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26178774-A-G

130094169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26178774-A-T

http://identifiers.org/hco/6/GRCh38#130094198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26178729-C-A

130094198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26178729-C-T

130094844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26178053-T-C

130095134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26177758-A-G

http://identifiers.org/hco/6/GRCh38#130095146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26177746-C-A

130095146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26177746-C-T

130095348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26177329-G-T

130095503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26177086-G-A

130096203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26176684-T-C

130096274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26176602-G-T

http://identifiers.org/hco/6/GRCh38#130096362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26176533-C-A

130096371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26176524-C-T

130096523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26176151-C-T

130096604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26176076-G-A

130096604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26176076-G-T

130096654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26176034-G-A

130096722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26175994-T-C

130096742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26175974-C-T

130097049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26175666-T-C

130097129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26175599-C-T

130097433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26175297-G-T

130097528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26175201-A-G

130097756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26175015-G-A

130097819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26174975-G-A

130098236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26174850-T-C

130098288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26174803-C-T

130098348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26174748-G-T

130098410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26174715-G-A

130098446-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26174682-C-G

130098446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26174682-C-T

130098665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26174475-G-C

130098840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26174317-T-C

130098935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26174263-A-G

130099123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26174124-T-G

130099322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26173922-G-C

130099481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26173768-T-G

130099528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26173564-A-G

130099572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26173521-A-T

130099852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26173269-G-A

130100009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26173113-A-G

http://identifiers.org/hco/6/GRCh38#130100140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26172972-A-C

130100209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26172910-G-A

130100264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26172883-C-T

130100362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26172784-C-T

130100648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26172519-A-G

130101371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26172190-G-A

130101426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26172128-T-A

130101741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26171845-G-C

130101792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26171798-G-A

130101803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26171787-T-C

130102039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26171566-A-G

130102977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26169992-G-C

130103170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26169805-A-T

130103174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26169801-A-G

130103459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26169536-A-T

130103483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26169512-G-T

130103757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26169235-A-G

130103932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26169100-C-T

130104297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26168796-T-G

http://identifiers.org/hco/6/GRCh38#130104346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26168756-C-A

130104346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26168756-C-T

130104347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26168755-T-C

130104347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26168755-T-G

130104357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26168745-A-G

130104466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense variant
orthologous variants: 26168649-G-T

http://identifiers.org/hco/6/GRCh38#130104506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26168609-C-A

130104506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense variant
orthologous variants: 26168609-C-G

130104506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense variant
orthologous variants: 26168609-C-T

130107240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26167015-G-A

130107317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26166938-A-G

130108568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26166228-A-G

130113226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26165281-G-A

130113226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26165281-G-C

130113471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26165109-C-T

130113514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26165066-G-A

130113627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, undefined
orthologous variants: 26164953-G-A

130113645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26164935-A-G

130113762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26164820-A-G

130113901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26164696-T-A

130113918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26164680-C-T

130114395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26164239-G-A

130114434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26164199-G-A

130114652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26163989-C-T

130114710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26163926-G-A

130114765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26163874-A-G

130114858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26163792-T-G

130115010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26163675-A-G

http://identifiers.org/hco/6/GRCh38#130115363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26163567-A-C

130115363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26163567-A-G

130115363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26163567-A-T

130115570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26163371-C-T

130115892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26163097-G-T

http://identifiers.org/hco/6/GRCh38#130116057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26162862-C-A

130116129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26162795-T-C

130116210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26162722-A-G

130116307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26162634-C-G

130116308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26162633-C-T

130116382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26162556-T-C

130118091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26161934-A-G

130118109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26161917-T-C

130118173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26161850-G-T

130118273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26161756-T-A

130118302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26161727-C-T

130118357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26161672-T-C

http://identifiers.org/hco/6/GRCh38#130118359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26161670-C-A

130118697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26161450-G-C

130119582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26160275-A-G

http://identifiers.org/hco/6/GRCh38#130119595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26160261-C-A

130119625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26160144-A-T

130120145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26159813-A-G

130120431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26159350-G-A

130120757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26158884-T-G

http://identifiers.org/hco/6/GRCh38#130120774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26158872-C-A

130120774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26158872-C-T

130120787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26158856-A-T

http://identifiers.org/hco/6/GRCh38#130120866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26158768-C-A

130120866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26158768-C-G

http://identifiers.org/hco/6/GRCh38#130120934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26158700-A-C

130120973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26158662-T-C

130121006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26158629-G-C

130121447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26158465-G-T

130121608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26158298-A-T

130133211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron variant
orthologous variants: 26156503-C-T

http://identifiers.org/hco/6/GRCh38#130133541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26155914-C-A

130133541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26155914-C-G

130133541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26155914-C-T

130134030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26155392-T-G

130134209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26155232-A-T

130139160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26152958-A-T

130139262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26152873-T-G

130139361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26152403-T-C

http://identifiers.org/hco/6/GRCh38#130139464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26152312-A-C

130139464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26152312-A-G

130139464-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26152312-A-T

130139550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26152221-A-G

130139568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26152204-T-C

130139581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26152191-C-T

http://identifiers.org/hco/6/GRCh38#130139857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26151912-A-C

130139857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26151912-A-G

130139947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26151828-G-A

130139947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26151828-G-T

http://identifiers.org/hco/6/GRCh38#130140066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26151710-C-A

130140066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26151710-C-G

130140066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26151710-C-T

130140211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26151568-G-T

130140610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26151176-G-C

130140610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26151176-G-T

130140661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26151131-G-A

130140703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26151089-T-G

130140721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26151071-T-C

130140755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26151040-T-C

130140842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26150955-G-A

130141036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26150758-T-C

http://identifiers.org/hco/6/GRCh38#130141039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#26150755-C-A

130141378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23035
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26150425-A-G