http://identifiers.org/hco/10/GRCh38#17951854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14393143-C-A

17952199-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14393467-G-C

17952234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14393502-G-A

17953054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14393940-T-A

17953054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14393940-T-C

17953054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14393940-T-G

http://identifiers.org/hco/10/GRCh38#17953116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14393985-C-A

17953116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14393985-C-T

http://identifiers.org/hco/10/GRCh38#17953177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14394040-C-A

17953177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394040-C-T

17953181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394044-T-C

17953228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 14394092-A-G

17953332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, missense_variant
orthologous variants: 14394187-G-T

17953334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, missense_variant
orthologous variants: 14394189-C-G

17953334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, missense_variant
orthologous variants: 14394189-C-T

17953428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, missense_variant
orthologous variants: 14394280-C-G

17953471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, missense_variant
orthologous variants: 14394323-C-G

17953471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 14394323-C-T

17953480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 14394332-G-A

17953480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, missense_variant
orthologous variants: 14394332-G-T

17953615-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394466-T-A

http://identifiers.org/hco/10/GRCh38#17953620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14394471-C-A

17953620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394471-C-T

17953635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394486-A-G

17953655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394503-G-A

17953655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394503-G-T

http://identifiers.org/hco/10/GRCh38#17953661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14394509-C-A

17953661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394509-C-T

17953794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394625-G-A

17953795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394626-C-T

17953821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394654-G-A

17953821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394654-G-T

http://identifiers.org/hco/10/GRCh38#17953841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14394674-A-C

17953889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394724-T-G

17954029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394872-A-G

17954131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14394991-A-G

17954551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14395380-G-A

17954812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14395688-A-G

17955401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14396285-C-T

17955446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14396331-A-G

17955503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14396388-C-T

17955596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14396477-G-A

17955619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14396499-T-G

http://identifiers.org/hco/10/GRCh38#17955700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14396571-C-A

17955700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14396571-C-T

http://identifiers.org/hco/10/GRCh38#17955817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14396669-C-A

17955829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14396681-T-C

17958768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14398070-C-T

17958950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14398251-G-A

17959066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14398393-A-G

17959066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14398393-A-T

17959510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14398750-C-T

17959715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14398930-G-A

17959772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14398985-T-C

17959814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14399027-C-T

17959819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14399030-C-T

17959863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14399070-G-A

17959933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14399143-T-C

17960189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14399403-A-G

17960254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14399461-G-A

17960387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14399590-C-G

17960450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14399654-A-G

17960543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14399748-G-A

17960543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14399748-G-C

17960659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14399854-A-G

17960668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14399862-A-T

17960741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14399921-C-T

17961114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14400488-A-G

17961172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14400550-G-A

http://identifiers.org/hco/10/GRCh38#17961431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14400741-C-A

17961441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14400752-G-A

17961441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14400752-G-T

17961480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14400790-T-A

17961480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14400790-T-G

17961545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14400847-T-A

17961568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14400870-T-A

17961631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 14400933-T-A

17961631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 14400933-T-C

17961649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 14400951-G-A

17961934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14401214-T-C

17961981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14401261-G-A

17961981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14401261-G-T

http://identifiers.org/hco/10/GRCh38#17962008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14401282-C-A

17962008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14401282-C-T

17962048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14401314-A-G

17962209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14401451-A-G

17962274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14401511-A-G

17962280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14401517-A-G

17962316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14401552-C-G

17962529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14401716-T-C

17963239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14402800-G-A

17963433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14403005-G-C

17963479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14403048-T-C

17963502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14403071-G-T

17963615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14403177-T-C

17963615-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14403177-T-G

http://identifiers.org/hco/10/GRCh38#17963773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14403312-C-A

17963873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14403419-C-T

17964006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14403519-C-T

17964209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14403695-G-A

17964273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14403757-C-T

17964388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14403904-A-G

17964437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14403951-C-T

17964481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14403991-C-T

17964758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14404280-G-A

17964780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14404301-C-T

17964798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14404314-C-G

17964986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14404521-C-T

http://identifiers.org/hco/10/GRCh38#17965096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14404647-A-C

17965096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14404647-A-G

17965110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14404665-G-A

http://identifiers.org/hco/10/GRCh38#17965205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14404750-C-A

17965205-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14404750-C-G

17965205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14404750-C-T

17965447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14404923-G-A

17965447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14404923-G-C

17965447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14404923-G-T

17965547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14405014-G-A

http://identifiers.org/hco/10/GRCh38#17965753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14405222-C-A

17966174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14406204-G-T

17966279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14406326-A-G

http://identifiers.org/hco/10/GRCh38#17966292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14406338-C-A

17976809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14408456-G-T

17976990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14408632-C-T

17977095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14408686-T-C

17977285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14408867-A-G

17977309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14408893-T-C

17977315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14408899-G-T

17977500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14409149-C-T

17977813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14409582-G-T

http://identifiers.org/hco/10/GRCh38#17977863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14409715-C-A

17977863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14409715-C-G

http://identifiers.org/hco/10/GRCh38#17977878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14409730-C-A

17977878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14409730-C-G

http://identifiers.org/hco/10/GRCh38#17977948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14409800-C-A

17977948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14409800-C-G

http://identifiers.org/hco/10/GRCh38#17977982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14409837-C-A

17977982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14409837-C-G

17977982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: stop gained
orthologous variants: 14409837-C-T

17978049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14409901-A-G

17978049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14409901-A-T

17978069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14409921-G-A

17978069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14409921-G-C

17978069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14409921-G-T

17978112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14409962-T-C

17978120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14409970-G-A

17978138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14409985-T-C

17978149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14409987-T-C

17978150-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14409988-T-A

17978151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14409989-G-A

17978151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14409989-G-T

17978152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14409990-T-A

17978152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14409990-T-C

17978323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14410143-A-G

17980540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14411608-G-T

17980545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14411613-C-T

17980785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14411835-T-A

17981047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14412093-C-G

17981274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14412216-G-T

http://identifiers.org/hco/10/GRCh38#17981288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14412230-C-A

17981288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14412230-C-T

17981291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14412233-T-C

17981361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14412303-T-C

http://identifiers.org/hco/10/GRCh38#17981365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14412307-A-C

17981365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: 14412307-A-G

17981365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: 14412307-A-T

17981389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: 14412331-G-A

http://identifiers.org/hco/10/GRCh38#17981410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14412352-C-A

http://identifiers.org/hco/10/GRCh38#17981458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14412400-A-C

17981532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14412465-A-T

17981540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14412473-A-G

17981551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14412484-G-A

17981551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14412484-G-C

17981551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14412484-G-T

http://identifiers.org/hco/10/GRCh38#17981620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14412551-A-C

17981620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14412551-A-G

17981688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14412619-G-C

17981742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14412674-G-T

17982056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14413450-T-G

http://identifiers.org/hco/10/GRCh38#17982145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14413538-A-C

17982150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14413543-C-T

17982199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14413592-C-G

17982206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14413597-C-G

17982278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14413659-G-A

17982285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14413666-A-G

http://identifiers.org/hco/10/GRCh38#17982435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14413846-C-A

17982470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14413880-G-A

17982633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14414049-T-C

17982633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14414049-T-G

17982639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14414055-G-A

17982723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14414128-G-T

17982728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14414134-G-A

17982752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14414158-G-A

17984172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14414450-T-A

17984172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14414450-T-C

http://identifiers.org/hco/10/GRCh38#17984211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#14414488-C-A

17984211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14414488-C-T

17984247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14414524-C-G

17984247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14414524-C-T

17984420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14414658-T-A

17984423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14414661-G-C

17984562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14414774-G-A

17984562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14414774-G-T

17984582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14414794-T-G

17984741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14415074-C-T

http://identifiers.org/hco/10/GRCh38#17984758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14415101-A-C

http://identifiers.org/hco/10/GRCh38#17984770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#14415113-A-C

17985855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14423934-G-A

http://identifiers.org/hco/10/GRCh38#17985970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14424032-A-C

17985970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424032-A-G

17986098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424159-C-G

http://identifiers.org/hco/10/GRCh38#17986104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14424165-C-A

17986104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424165-C-G

17986107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424168-A-G

17986308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424378-A-G

17986326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424399-T-C

17986408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424475-G-T

17986475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424553-C-G

17986531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424604-C-G

17986531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424604-C-T

http://identifiers.org/hco/10/GRCh38#17986568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14424635-C-A

17987418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424807-A-G

http://identifiers.org/hco/10/GRCh38#17987426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14424815-C-A

17987426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424815-C-T

17987436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424825-G-A

17987436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424825-G-C

17987441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424830-C-G

17987441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14424830-C-T

http://identifiers.org/hco/10/GRCh38#17987516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14424904-A-C

17987540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: 14424928-G-A

17987540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: 14424928-G-T

17987737-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14425101-T-A

17987737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14425101-T-C

http://identifiers.org/hco/10/GRCh38#17987764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14425129-C-A

17987764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14425129-C-T

17987813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14425177-C-T

17989164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14426224-G-T

http://identifiers.org/hco/10/GRCh38#17989224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14426283-C-A

http://identifiers.org/hco/10/GRCh38#17989912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#14426639-C-A

17989912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14426639-C-T

17989943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14426664-T-G

17989994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14426712-T-G

17990265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14426990-G-A

17990456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14427448-A-G

17990479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14427469-G-A

17990486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14427476-G-A

17990761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14427668-A-G

17990806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14427702-A-G

17990923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14427807-T-C

17990935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14427819-T-C

17990975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14427857-G-A

17991012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14427884-A-G

http://identifiers.org/hco/10/GRCh38#17991066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14427931-C-A

17991066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14427931-C-T

http://identifiers.org/hco/10/GRCh38#17991073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14427938-C-A

17991073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14427938-C-G

17991073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14427938-C-T

17991076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14427941-A-G

17991134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14439000-T-C

17991157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14439023-G-A

17991157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14439023-G-C

17991157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14439023-G-T

17991184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14439047-T-C

17991195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14439058-C-G

17991195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: 14439058-C-T

17991213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: 14439076-T-C

http://identifiers.org/hco/10/GRCh38#17991355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14439210-C-A

17991355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14439210-C-T

17991378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14439232-G-T

17991384-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14439238-A-T

17992778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440012-G-A

17992910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440138-T-C

http://identifiers.org/hco/10/GRCh38#17992986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14440215-A-C

17993036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440264-G-A

17993036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440264-G-C

17993109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440396-A-G

http://identifiers.org/hco/10/GRCh38#17993132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14440419-A-C

17993186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 14440472-C-T

17993204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 14440490-G-A

17993219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 14440505-C-T

17993234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 14440520-C-T

17993295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440581-G-A

17993295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440581-G-C

17993295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440581-G-T

http://identifiers.org/hco/10/GRCh38#17993312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14440598-A-C

http://identifiers.org/hco/10/GRCh38#17993317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14440603-A-C

17993317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440603-A-G

17993317-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440603-A-T

http://identifiers.org/hco/10/GRCh38#17993330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14440616-C-A

17993330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440616-C-T

http://identifiers.org/hco/10/GRCh38#17993356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14440639-C-A

17993356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440639-C-G

17993360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440643-T-A

17993391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440671-A-G

17993414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14440694-A-G

17993751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14441049-G-A

17993828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14441123-A-G

17993828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14441123-A-T

17993952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14441224-T-C

17994094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14441435-G-A

17994222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14441659-C-G

17994979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14448197-G-A

http://identifiers.org/hco/10/GRCh38#17995139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14448335-C-A

17995139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14448335-C-T

17995398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14448586-A-G

17995405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14448593-A-T

17995498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14448664-C-T

http://identifiers.org/hco/10/GRCh38#17995524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14448691-C-A

17995539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14448707-A-T

17995691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: 14448858-T-A

17995691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous variant
orthologous variants: 14448858-T-C

17995692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: missense variant
orthologous variants: 14448859-A-G

17996284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14450368-C-T

17996373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14450447-A-G

17996381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14450455-C-G

17996433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14450500-A-G

17996725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14450815-C-T

17996749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14450846-G-C

17997448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14451434-A-G

17997836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14451806-G-A

17997867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14451835-G-T

17997955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14451922-T-A

17997955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14451922-T-C

17998342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14452177-A-G

17998429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14452266-A-T

17998462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14452296-G-A

http://identifiers.org/hco/10/GRCh38#17999366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14452971-C-A

17999504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14453094-A-G

17999548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14453135-A-G

17999576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14453175-C-T

17999580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14453179-C-G

17999701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14453302-A-G

17999701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14453302-A-T

17999803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14453404-G-A

http://identifiers.org/hco/10/GRCh38#18000006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14453607-C-A

18000129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14453726-C-T

18000203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14453811-C-T

18000497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14454401-A-G

18000546-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14454449-A-T

18000638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14454549-G-A

18000638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14454549-G-C

18000642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14454553-C-T

18000900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14454793-G-A

18000900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14454793-G-T

http://identifiers.org/hco/10/GRCh38#18000941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14454854-C-A

18000941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14454854-C-T

18002225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14455813-C-T

18002282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14455871-A-T

18002287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14455876-C-T

18002290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14455879-G-T

18002341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14455916-C-T

18002461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456032-G-T

http://identifiers.org/hco/10/GRCh38#18002499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#14456070-C-A

18002499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456070-C-T

18002508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456079-G-A

18002520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456091-A-G

18002547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456117-G-A

18002547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456117-G-C

18002547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456117-G-T

18002640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456217-T-G

http://identifiers.org/hco/10/GRCh38#18002764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#14456350-C-A

18002764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456350-C-T

18002777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456363-T-C

18002808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456393-G-A

18002829-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456428-A-T

18002849-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456448-T-A

18002875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456476-G-A

18002875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456476-G-T

18002902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456503-C-G

18002957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456552-G-T

18003064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456647-A-G

http://identifiers.org/hco/10/GRCh38#18003075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#14456658-C-A

18003075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456658-C-T

http://identifiers.org/hco/10/GRCh38#18003096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#14456681-C-A

18003096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456681-C-G

http://identifiers.org/hco/10/GRCh38#18003122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#14456707-C-A

18003122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14456707-C-T

http://identifiers.org/hco/10/GRCh38#18003292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#14456888-A-C

18003292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous_variant, undefined
orthologous variants: 14456888-A-G

18003346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: synonymous_variant, undefined
orthologous variants: 14456942-C-T

18003437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14457030-A-G

18003497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14457103-T-G

18003526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14457132-G-A

18003526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14457132-G-T

18003634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14457185-G-A

18003675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14457219-T-C

18003679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14457223-C-T

18003680-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14457224-T-G

18003993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14457457-A-G

18004206-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14457968-A-T

18004481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14458235-A-G

18005595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14459806-A-G

18005696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14459906-T-C

18005706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14459916-C-T

18005782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14459983-G-C

18005783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14459984-G-A

http://identifiers.org/hco/10/GRCh38#18005819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#14460021-C-A

18005819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14460021-C-T

18005823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14460025-G-A

18006382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14460561-A-G

18008923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14469132-T-A

http://identifiers.org/hco/10/GRCh38#18009017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#14469224-C-A

http://identifiers.org/hco/10/GRCh38#18009056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#14469264-A-C

18009056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14469264-A-G

18009068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14469276-A-T

18009463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14470009-C-G

18009574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14470106-T-C

18009650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14470153-G-A

18009650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron_variant, undefined
orthologous variants: 14470153-G-T

18014135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14471454-C-T

18014136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14471455-A-T

18014137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14471456-A-G

18014235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14471569-T-A

18014235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14471569-T-G

18014237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14471571-C-T

18014293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14471616-G-A

18014368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14471691-A-G

18014368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14471691-A-T

18015272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14472146-T-C

18015293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14472168-A-G

18015296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14472171-T-C

18029486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14488739-G-A

18029490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14488743-T-C

18029538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14488790-G-C

18029579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14488830-G-C

18029698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14495131-C-G

18029774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14495202-G-C

http://identifiers.org/hco/10/GRCh38#18029962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14495363-C-A

18030048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14495454-T-A

18030125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14495523-T-A

18030131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14495529-C-T

18030133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14495530-T-A

18030133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14495530-T-C

18030155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14495552-G-A

18030169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14495566-A-G

18037359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14495853-C-T

18039334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14498236-T-C

18039442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14498305-T-G

http://identifiers.org/hco/10/GRCh38#18041059-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14498556-A-C

18041179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14498671-C-T

18041233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14498725-A-G

18042099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14498927-G-C

18042148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14498975-G-C

http://identifiers.org/hco/10/GRCh38#18042626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14499153-C-A

18042626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14499153-C-G

18042626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: intron variant
orthologous variants: 14499153-C-T

18042847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: 3 prime UTR variant
orthologous variants: 14499375-A-T

18042909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: 3 prime UTR variant
orthologous variants: 14499435-T-A

18042909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: 3 prime UTR variant
orthologous variants: 14499435-T-C

18042917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: 3 prime UTR variant
orthologous variants: 14499443-T-C

18042934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: 3 prime UTR variant
orthologous variants: 14499458-T-C

http://identifiers.org/hco/10/GRCh38#18043135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#14499641-C-A

18043144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: 3 prime UTR variant
orthologous variants: 14499650-G-C

18043266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20860
most severe consequence: 3 prime UTR variant
orthologous variants: 14499765-G-T