45574203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, undefined
orthologous variants: 7013267-G-A

45574203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, undefined
orthologous variants: 7013267-G-C

45574203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, undefined
orthologous variants: 7013267-G-T

45574249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7013311-G-A

45574249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7013311-G-C

45574249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7013311-G-T

45574376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7013438-C-G

45574376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 7013438-C-T

http://identifiers.org/hco/7/GRCh38#45574469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7013524-C-A

45574469-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7013524-C-G

45574469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 7013524-C-T

45574767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, missense_variant
orthologous variants: 7013820-T-C

45574771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 7013824-G-A

45574771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 7013824-G-T

45574807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 7013860-C-G

45574807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 7013860-C-T

45574861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 7013914-C-G

45574861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 7013914-C-T

45574864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 7013917-G-T

45574927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 7013980-C-T

45574993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 7014046-C-T

45575020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 7014073-C-G

45575020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 7014073-C-T

45575143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 7014196-C-T

http://identifiers.org/hco/7/GRCh38#45575158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7014211-C-A

45575158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 7014211-C-T

45575196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, undefined
orthologous variants: 7014249-C-T

45575209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, undefined
orthologous variants: 7014262-T-C

45575209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, undefined
orthologous variants: 7014262-T-G

http://identifiers.org/hco/7/GRCh38#45575325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7014374-C-A

45575325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7014374-C-T

45575478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7014531-G-T

http://identifiers.org/hco/7/GRCh38#45575479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7014532-C-A

45575479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7014532-C-T

45575594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7014652-G-A

45575883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7014934-G-A

45575904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7014960-C-T

45575936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7014991-C-G

45576012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7015070-C-G

45576085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7015100-T-G

45576127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7015135-T-C

45577441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7015941-A-G

45577538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7015992-T-A

45577604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7016057-C-G

45577780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7016203-G-T

45577783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7016206-C-T

45577784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7016207-T-G

45577791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7016214-A-G

45577948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7016348-C-T

http://identifiers.org/hco/7/GRCh38#45577997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7016387-C-A

http://identifiers.org/hco/7/GRCh38#45578689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7016503-C-A

http://identifiers.org/hco/7/GRCh38#45578739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7016551-A-C

45578902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7016721-G-T

45579002-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7016822-T-A

45580857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7016859-G-A

45580866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7016868-T-C

45580866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7016868-T-G

http://identifiers.org/hco/7/GRCh38#45581337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7017314-A-C

45581743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7017651-C-T

45581749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7017674-A-G

45581851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7017777-A-G

45582043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7017987-A-T

45582238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7018194-C-T

45582373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7018341-A-G

45582521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7018462-G-A

45582724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7018605-T-C

45582796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7018658-C-T

45582797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7018659-G-A

45582928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7018715-C-T

45583220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7018924-T-C

45583269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7018971-G-A

45583383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7019067-C-T

45583427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7019108-A-G

45583489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7019152-G-T

45584267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7019281-A-G

45584578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7019581-C-G

http://identifiers.org/hco/7/GRCh38#45584782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7019801-C-A

45585113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7020149-A-G

45585140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7020178-A-G

45585289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7020317-T-C

45585294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7020322-T-G

http://identifiers.org/hco/7/GRCh38#45585885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7020514-A-C

45586095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7020702-T-C

45586241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7020844-T-C

45586324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7020923-T-C

http://identifiers.org/hco/7/GRCh38#45586396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7020994-A-C

http://identifiers.org/hco/7/GRCh38#45586478-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7021071-A-C

45586502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7021094-T-C

45586802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7021398-A-G

45586897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7021488-T-C

http://identifiers.org/hco/7/GRCh38#45587130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7021707-A-C

45587248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7021802-G-A

45587248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7021802-G-C

45587253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7021813-A-G

45587291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7021851-G-A

45587432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7022030-C-G

45587432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7022030-C-T

45587524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7022109-T-C

45587648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7022256-G-C

45588343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7022864-A-G

45588407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7022949-C-G

http://identifiers.org/hco/7/GRCh38#45588503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7023106-A-C

45588503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7023106-A-G

http://identifiers.org/hco/7/GRCh38#45588515-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7023117-A-C

45588517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7023119-A-G

45588672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7023303-C-T

45588690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7023321-G-A

45588706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7023339-T-C

45588786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7023433-G-A

45589627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7024427-A-G

45589644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7024435-G-T

45589662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7024453-G-A

45589874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7024771-G-A

45590026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7024949-T-G

45590078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7024989-C-T

45590084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7024990-A-G

45590124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7025030-C-T

45590340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7025218-T-C

45590421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7025297-C-T

45590706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7026833-G-C

45591276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7027490-G-T

45591303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7027515-C-T

45591673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7027807-A-G

45591681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7027815-G-T

45592060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7028206-T-G

http://identifiers.org/hco/7/GRCh38#45592409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7028499-C-A

45592409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7028499-C-T

45592560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7028668-T-C

45592599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7028709-C-G

45592654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7028752-G-A

45592654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7028752-G-T

45592656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7028754-C-G

45592656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7028754-C-T

45592717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7028845-G-A

45592735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7028864-T-C

45592743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7028872-C-G

45592743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7028872-C-T

45592763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 7028892-G-T

45593030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7029205-A-G

45593157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7029316-G-A

45593228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7029383-C-G

45593228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7029383-C-T

http://identifiers.org/hco/7/GRCh38#45593591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7029623-C-A

45593619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7029652-G-T

45593944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7029962-C-T

45594092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7030102-T-C

45594101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7030116-C-G

45594443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7030445-C-T

45594526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7030531-C-T

45594537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7030542-T-A

45594577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7030586-T-C

45596900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7032932-A-G

45596971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7032998-A-G

45597181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7033183-C-T

45597215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7033219-G-T

45597273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7033281-C-T

45597376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7033360-C-T

45597412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7033392-G-A

45597896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7034390-T-G

45598108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7034567-G-A

45598140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7034607-T-G

http://identifiers.org/hco/7/GRCh38#45598156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7034623-A-C

45598166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7034633-C-T

45598408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7034835-T-C

45598620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7035048-T-C

45598712-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7035262-C-G

45598812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7035350-G-A

http://identifiers.org/hco/7/GRCh38#45599011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7035562-C-A

45599031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7035575-C-T

http://identifiers.org/hco/7/GRCh38#45599977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7036621-A-C

45599989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7036633-A-G

45599995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7036639-G-A

45600083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7036727-G-A

http://identifiers.org/hco/7/GRCh38#45600218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7036861-C-A

45600299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7036945-C-T

45600371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7037004-C-G

45601134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7038021-G-A

http://identifiers.org/hco/7/GRCh38#45601496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7038331-C-A

45601496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7038331-C-G

45601496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7038331-C-T

45601567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7038396-G-A

45601622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7038456-C-T

http://identifiers.org/hco/7/GRCh38#45601863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7038675-C-A

45602065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7038877-G-C

45602065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7038877-G-T

45602273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7039143-C-G

45602280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7039150-G-C

45602296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7039167-G-C

45602304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7039175-C-T

45602314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7039185-G-A

45602322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7039193-G-A

45602852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7039966-T-C

45602961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7040092-C-T

45603027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7040154-G-A

45605803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7046186-T-C

45606280-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7046450-T-G

45606281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7046451-G-C

45606471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7046644-A-G

45606488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7046659-G-T

45606795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7047291-A-G

45606799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7047295-G-A

45606902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7047399-C-T

45606955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7047447-G-A

45608824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7049113-G-A

45608912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7049169-C-T

45608919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7049178-C-T

45609098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7049332-A-T

45609105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7049339-A-G

45609187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7049401-C-T

45609217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7049430-G-A

45609297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7049498-C-T

http://identifiers.org/hco/7/GRCh38#45609507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7049678-C-A

45609507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7049678-C-T

45609625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7049789-A-G

45609731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7049883-A-G

45609757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7049907-A-G

45610042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050215-G-T

45610092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050265-G-T

45610174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050322-G-A

45610174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050322-G-T

45610177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050325-G-A

45610189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050338-G-A

http://identifiers.org/hco/7/GRCh38#45610240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7050388-C-A

45610240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050388-C-T

http://identifiers.org/hco/7/GRCh38#45610273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7050421-C-A

45610273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050421-C-T

http://identifiers.org/hco/7/GRCh38#45610274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7050422-C-A

45610275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050423-T-C

http://identifiers.org/hco/7/GRCh38#45610283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7050430-C-A

45610283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050430-C-T

45610290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050437-G-A

45610290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050437-G-T

45610330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050526-G-A

45610330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050526-G-T

45610343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050535-C-T

45610447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: synonymous variant
orthologous variants: 7050638-C-G

45610447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: synonymous variant
orthologous variants: 7050638-C-T

http://identifiers.org/hco/7/GRCh38#45610538-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7050742-A-C

45610567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050767-G-T

45610569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050769-G-A

45610609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050809-G-A

45610627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050827-G-A

45610627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050827-G-T

45610631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050831-G-A

45610631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050831-G-T

45610662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050863-A-G

45610662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050863-A-T

45610706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7050913-G-T

45611455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7051073-A-G

45611511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7051108-G-A

45611653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7051241-A-G

45611653-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7051241-A-T

45611706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7051295-A-G

45611814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7051394-T-C

45611839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7051417-T-C

45611844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7051422-G-C

45612022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7051574-C-T

45612168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7051708-A-T

45612182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7051722-G-T

http://identifiers.org/hco/7/GRCh38#45612266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7051870-A-C

45620365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7056869-C-T

45620413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7056919-T-C

45620603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7057118-T-C

45620630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7057142-A-G

45620649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7057161-A-G

45620650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7057162-A-G

45620650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7057162-A-T

45620792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7057292-G-A

45620841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7057344-A-G

45620858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7057356-T-G

http://identifiers.org/hco/7/GRCh38#45621026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7057513-C-A

45621512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058034-G-A

45621567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058075-G-A

45621588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058101-G-A

45621644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058138-C-T

45621659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058157-T-A

45621758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058256-C-T

45621774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058276-A-G

45622068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058516-T-G

45622069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058517-T-G

45622238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058627-G-A

45622279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058671-G-A

45622279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058671-G-T

45622299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058697-G-A

45622353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058748-T-C

45622379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058773-G-T

45622490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058882-G-A

45622490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058882-G-T

45622529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058916-A-G

45622591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058961-T-C

http://identifiers.org/hco/7/GRCh38#45622619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7058988-C-A

45622619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7058988-C-T

45622677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: missense variant
orthologous variants: 7059046-G-C

45622753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7059122-G-A

45622801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7059168-T-G

45622807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7059174-A-G

45622810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7059177-T-C

45622810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7059177-T-G

45622834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7059200-A-G

45622834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7059200-A-T

45622901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7059211-G-A

45623066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7059326-T-C

45623135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7059401-T-G

45623821-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7059838-T-G

45623831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7059855-G-C

45624176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7060118-C-T

45624219-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7060152-T-G

45624283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7060227-T-G

45624358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7060288-A-G

45624358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7060288-A-T

http://identifiers.org/hco/7/GRCh38#45626443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7062031-C-A

45626614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7062215-G-A

45626848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7062447-C-T

45627160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7062730-C-T

45627245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7062787-A-T

45627442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7062955-G-C

45627513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7063030-G-C

45627778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7063294-A-G

45627844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7063379-C-T

45628021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7063538-G-T

45628022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7063539-G-A

45628080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7063588-G-T

45628270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7063763-C-G

45628317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7063805-G-A

45628560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7063964-C-T

45628710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7064091-C-G

45628791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7064189-T-G

45628832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7064232-C-G

45631057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7066519-G-C

45631077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7066539-G-A

45631157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7066625-T-C

45631502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7066938-A-G

http://identifiers.org/hco/7/GRCh38#45631871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7067333-A-C

45631996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7067420-G-A

45632412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7067788-G-A

45632440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7067817-C-T

http://identifiers.org/hco/7/GRCh38#45639341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7072389-C-A

45639528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7072578-C-T

45639614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7072635-G-T

45639810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7072816-C-T

45639866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7072865-T-C

45639953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7072943-T-C

45640935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7073637-C-G

45640954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7073657-T-A

45641082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7073780-A-T

45641083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7073781-T-G

http://identifiers.org/hco/7/GRCh38#45643417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7075484-A-C

45643424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7075491-G-T

45643559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7075610-G-A

45643579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7075630-G-T

45643717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7075772-A-G

http://identifiers.org/hco/7/GRCh38#45643893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7075965-C-A

45643926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7076001-A-T

45644034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7076175-C-T

45644450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7076971-A-G

45648617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7080229-C-T

45648650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7080256-T-C

45648750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7080356-T-C

45648958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080464-G-C

45648961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080467-T-A

45648991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080497-T-A

45648995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080501-G-A

45649083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080580-A-G

45649247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7080715-G-A

45650649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082334-G-A

http://identifiers.org/hco/7/GRCh38#45650834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7082508-A-C

45651133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082723-C-T

45651208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7082785-C-T

45651508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7083067-A-G

45651555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7083116-C-T

45651621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7083159-A-G

45651695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7083230-A-G

45651755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7083282-C-T

http://identifiers.org/hco/7/GRCh38#45651786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7083313-A-C

45654197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7084642-T-C

45654235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7084678-C-G

45654439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7084869-T-C

45654776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7085146-G-A

45655306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7085624-A-T

45655543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7085821-A-G

45655749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086021-A-G

45655929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086195-A-G

45656776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086677-C-G

45656798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086703-C-T

45656802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086707-A-G

45656832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086755-C-G

45656848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086771-C-T

45656854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086777-G-A

45656854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086777-G-C

45656873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086804-G-A

45657002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7086907-C-T

45657646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7087191-A-G

45657660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7087205-G-A

45657660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7087205-G-C

45657660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7087205-G-T

45657992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7087513-G-A

45657992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7087513-G-T

45658014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7087527-G-A

http://identifiers.org/hco/7/GRCh38#45658145-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7087586-A-C

45658257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7087678-A-G

45658282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7087699-C-G

45659898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088146-T-C

45659957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088207-G-T

45660051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7088296-T-C

45660063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7088308-G-A

45660063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7088308-G-T

45660090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7088335-C-T

http://identifiers.org/hco/7/GRCh38#45660230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7088471-C-A

45660230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088471-C-T

http://identifiers.org/hco/7/GRCh38#45660264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7088504-C-A

45660264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088504-C-T

45660271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088512-T-A

http://identifiers.org/hco/7/GRCh38#45660272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7088513-C-A

http://identifiers.org/hco/7/GRCh38#45660282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7088523-C-A

45660326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088542-A-G

45660367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088582-G-C

http://identifiers.org/hco/7/GRCh38#45660385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7088600-C-A

45660405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088624-T-G

45660446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7088657-C-T

45662236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089210-G-A

45662236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089210-G-T

45662246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089220-A-G

45662246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7089220-A-T

45665330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092242-T-C

45665526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092415-T-C

45665916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092813-G-A

45665953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7092842-A-G

45677275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094137-C-T

45677277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094139-G-C

45677320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094177-G-A

45677336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094193-C-G

45677462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094290-C-T

http://identifiers.org/hco/7/GRCh38#45677759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7094576-C-A

45677759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094576-C-T

45677790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094606-G-A

45677790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094606-G-T

45677841-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094650-T-A

45677841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094650-T-C

45677856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094665-A-G

45677858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094667-G-A

http://identifiers.org/hco/7/GRCh38#45677955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7094764-C-A

45677955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7094764-C-T

45678079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7094889-T-A

45678294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7095178-T-G

http://identifiers.org/hco/7/GRCh38#45678300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7095184-A-C

45678989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7095873-C-T

http://identifiers.org/hco/7/GRCh38#45679446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7096262-C-A

45679446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096262-C-T

45679474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096288-G-A

45679574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096375-G-A

45679574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096375-G-T

45679629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096431-G-T

45679635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096436-A-G

45679635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096436-A-T

45679937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096656-T-A

45679946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096660-T-C

45679994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096694-T-C

45680104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096759-A-G

45680165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096813-G-A

45680225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096868-G-C

http://identifiers.org/hco/7/GRCh38#45680270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7096901-C-A

45680270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096901-C-T

45680286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096912-G-T

45680303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096929-T-A

45680307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7096933-T-C

45680366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7096989-A-G

45680366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7096989-A-T

45680458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7097081-A-T

45680537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7097128-T-C

45681161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7097597-T-C

45681164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7097600-G-A

http://identifiers.org/hco/7/GRCh38#45681178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7097614-A-C

45684461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7098582-G-A

45684461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7098582-G-T

45684660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7098803-T-C

http://identifiers.org/hco/7/GRCh38#45684678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7098821-C-A

45684678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7098821-C-T

45684784-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7098952-T-A

45684784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7098952-T-C

45684785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7098953-A-T

45684792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7098966-G-A

45684792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7098966-G-T

45685093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099616-G-C

45685097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099620-T-C

45685746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099747-G-A

45685746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099747-G-T

45685790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099791-G-T

45685816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099815-A-G

45685816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099815-A-T

45685819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099818-T-C

45685829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099828-G-A

45685829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099828-G-C

45685829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099828-G-T

45685850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099859-G-A

45685850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099859-G-T

http://identifiers.org/hco/7/GRCh38#45685863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7099875-C-A

45685863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099875-C-T

45685895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099897-A-G

45685925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 7099927-G-T

45685988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 7099988-C-T

45686007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 7100007-C-G

45686165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: synonymous variant
orthologous variants: 7100165-C-T

45686227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100227-G-A

45686227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100227-G-C

45686227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100227-G-T

45686268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100464-T-G

45686278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100474-G-C

45686396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100631-G-T

45686398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100633-T-C

http://identifiers.org/hco/7/GRCh38#45686412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7100647-C-A

45686412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100647-C-T

45686542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 7100772-C-G

45686551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: missense variant
orthologous variants: 7100781-G-A

45686609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: missense variant
orthologous variants: 7100839-C-G

45686609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: missense variant
orthologous variants: 7100839-C-T

45686700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100927-G-A

45686700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100927-G-C

45686700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100927-G-T

45686709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100936-G-A

45686709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100936-G-T

http://identifiers.org/hco/7/GRCh38#45686763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7100963-A-C

45686771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100971-G-A

45686771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100971-G-T

45686778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100978-G-A

45686778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7100978-G-T

45686872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7101025-C-T

45687824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7101836-C-T

45687887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7101887-T-G

45687891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7101891-C-G

45688144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7102172-G-A

45688160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7102188-G-A

45688160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7102188-G-T

45690668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7102508-C-G

45690668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7102508-C-T

45690927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7102748-G-A

45690927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7102748-G-T

45691117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 7102936-G-A

45691307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 7103114-A-G

45691361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 7103174-T-C

45699885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7105365-C-T

45700002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7105435-G-C

45700188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7105600-A-G

45700489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7106250-A-G

45700625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7106360-A-T

45700655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7106390-A-G

45700695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7106424-T-A

45700806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7106517-T-C

45700842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7106557-A-G

45701030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7106742-G-T

45701097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7106807-G-A

45701097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7106807-G-C

45701426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7107073-G-A

45701504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7107755-A-G

45701665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7107904-G-T

45701953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7108267-C-T

45701956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7108270-G-C

45701957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7108271-C-G

45701957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7108271-C-T

http://identifiers.org/hco/7/GRCh38#45701965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7108279-A-C

45701965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7108279-A-G

45701971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7108280-A-G

45701979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7108288-C-T

45702278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7108537-C-G

45702337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7108577-C-T

45702587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7108865-G-C

45702605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7108883-G-A

45702605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7108883-G-T

45702710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7109081-G-T

45702736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7109106-C-T

45702756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7109120-G-A

45702756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7109120-G-C

45703050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7109299-G-A

45703141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7109371-T-A

45703291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7109498-T-G

http://identifiers.org/hco/7/GRCh38#45703453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7110283-C-A

45703453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: missense variant
orthologous variants: 7110283-C-G

45703453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: synonymous variant
orthologous variants: 7110283-C-T

http://identifiers.org/hco/7/GRCh38#45703868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7111485-C-A

45703868-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7111485-C-G

45703868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7111485-C-T

http://identifiers.org/hco/7/GRCh38#45703885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7111498-C-A

45703886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7111499-T-C

45703886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7111499-T-G

45703887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7111500-G-A

45703887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7111500-G-C

45703887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7111500-G-T

45704142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7111589-C-T

45704488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7111817-A-G

45704550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: synonymous variant
orthologous variants: 7111884-G-A

45704550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: missense variant
orthologous variants: 7111884-G-C

45704556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: missense variant
orthologous variants: 7111890-C-G

45704622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7111956-T-C

http://identifiers.org/hco/7/GRCh38#45704716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7112016-C-A

45704736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7112036-A-G

45704747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7112047-T-A

45704747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7112047-T-G

http://identifiers.org/hco/7/GRCh38#45704749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7112049-C-A

45704905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7112155-C-T

http://identifiers.org/hco/7/GRCh38#45704938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7112166-A-C

45705074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7112229-A-G

http://identifiers.org/hco/7/GRCh38#45705249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7112368-C-A

45705348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7112472-T-C

45705481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7112585-G-A

45705481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7112585-G-C

45705699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7112952-T-C

http://identifiers.org/hco/7/GRCh38#45705732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7112994-A-C

45706224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7113457-C-T

45706348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7113513-T-C

http://identifiers.org/hco/7/GRCh38#45706492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7113606-C-A

45706714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7113821-A-G

45706771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7113870-G-A

45706909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7114007-C-T

45706942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7114040-G-A

45706957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7114055-C-T

45706977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7114075-G-T

45707136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7114228-G-A

45707216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7114314-T-C

45707268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7114364-A-G

45707504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7114528-T-A

45707525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7114549-A-G

45708225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7115266-G-T

http://identifiers.org/hco/7/GRCh38#45708256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7115297-C-A

45708294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7115355-G-T

45708315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7115378-C-T

45708334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7115396-A-G

45708367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: synonymous variant
orthologous variants: 7115429-C-T

http://identifiers.org/hco/7/GRCh38#45708519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7115556-A-C

45710322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7116882-G-C

45710336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7116902-G-A

http://identifiers.org/hco/7/GRCh38#45710382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7116946-C-A

45710391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7116955-G-A

http://identifiers.org/hco/7/GRCh38#45710398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7116962-C-A

45710398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7116962-C-G

45710485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7117021-A-G

45710517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7117053-C-T

45710682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7117217-G-T

45710758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7117293-G-A

45710758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7117293-G-T

45710879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7117425-G-A

45710987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7117702-T-C

45713576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7119286-G-A

45713576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7119286-G-C

45713585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7119295-G-A

45713586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7119296-G-C

45713586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7119296-G-T

http://identifiers.org/hco/7/GRCh38#45713592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7119302-C-A

45713592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7119302-C-T

45713593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7119303-A-G

45713594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7119304-G-A

45713594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7119304-G-T

45713611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: intron variant
orthologous variants: 7119319-T-C

http://identifiers.org/hco/7/GRCh38#45714082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7119800-C-A

45714082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7119800-C-T

45714121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7119828-G-A

45714333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7119954-A-G

http://identifiers.org/hco/7/GRCh38#45714341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7119962-C-A

45714341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7119962-C-G

45714341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7119962-C-T

45714414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7120109-G-A

45714655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7120382-C-T

45714783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7120493-G-A

45714783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7120493-G-T

http://identifiers.org/hco/7/GRCh38#45714819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7120528-C-A

45714819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7120528-C-T

http://identifiers.org/hco/7/GRCh38#45714822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7120531-C-A

45714902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7120603-T-C

45714950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7120643-G-A

45714955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7120648-T-C

45715123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7120818-A-G

45715167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7120866-A-G

45715224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7120917-T-C

45715225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7120918-G-A

45715380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7120986-G-T

http://identifiers.org/hco/7/GRCh38#45715473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7121067-C-A

45715473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121067-C-T

45715521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121111-T-A

45715521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121111-T-C

45715523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121113-G-T

45715713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121186-G-A

45715727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121200-G-A

45715727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121200-G-T

45715766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121237-G-T

45715833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121302-T-C

45715833-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121302-T-G

http://identifiers.org/hco/7/GRCh38#45715839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7121312-C-A

45715839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121312-C-T

http://identifiers.org/hco/7/GRCh38#45715840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7121313-C-A

45715854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121336-T-C

45715855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121337-G-A

45715855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121337-G-T

45715867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121370-G-T

45715888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121395-G-T

45715893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121400-G-T

45715978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121494-G-A

45715978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121494-G-T

45716067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121614-G-T

http://identifiers.org/hco/7/GRCh38#45716098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7121638-C-A

45716098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121638-C-T

45716219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121756-T-C

45716266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121791-G-T

45716306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121818-G-C

45716306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121818-G-T

http://identifiers.org/hco/7/GRCh38#45716319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7121829-C-A

45716319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121829-C-T

http://identifiers.org/hco/7/GRCh38#45716323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7121833-C-A

45716323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121833-C-T

45716354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121865-G-A

45716354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121865-G-T

45716493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7121986-G-T

http://identifiers.org/hco/7/GRCh38#45716615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7122103-C-A

45716615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7122103-C-G

45716615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7122103-C-T

45716649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7122135-G-T

http://identifiers.org/hco/7/GRCh38#45716721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7122199-A-C

45716852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7122327-C-G

45716852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7122327-C-T

45716955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7122421-G-T

45716971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7122438-A-G

http://identifiers.org/hco/7/GRCh38#45717069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7122531-C-A

45717069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7122531-C-T

45717166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7122636-T-C

http://identifiers.org/hco/7/GRCh38#45717327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7122786-C-A

45717655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7123113-G-A

45717655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7123113-G-T

45717675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7123133-G-T

http://identifiers.org/hco/7/GRCh38#45717698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7123156-C-A

45717802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7123258-G-A

45717802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7123258-G-T

45718119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7123534-G-T

45718198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7123594-C-T

http://identifiers.org/hco/7/GRCh38#45718575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7124690-C-A

45718575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124690-C-T

45718597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124712-G-A

45718635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124745-G-T

45718644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124754-G-A

45718703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124804-G-A

45718703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124804-G-T

http://identifiers.org/hco/7/GRCh38#45718704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7124805-C-A

45718704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124805-C-T

45718727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124828-G-A

45718727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124828-G-T

45718787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124876-G-A

45718787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124876-G-T

45718828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124915-T-C

45718859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124949-G-A

45718859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124949-G-T

45718876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124964-G-A

45718876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124964-G-T

45718896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124984-G-A

45718896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7124984-G-T

http://identifiers.org/hco/7/GRCh38#45719317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7125270-A-C

45719334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7125284-T-C

45719417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7125345-G-A

45719417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7125345-G-T

45719591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7125527-C-T

45719657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7125592-T-C

http://identifiers.org/hco/7/GRCh38#45719822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7125742-C-A

45719822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7125742-C-T

http://identifiers.org/hco/7/GRCh38#45719824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7125744-C-A

http://identifiers.org/hco/7/GRCh38#45720594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7126215-C-A

45720594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7126215-C-T

http://identifiers.org/hco/7/GRCh38#45720669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7126267-C-A

45720711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7126297-G-A

45720711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7126297-G-T

45720727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7126313-T-C

45720727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7126313-T-G

45720756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7126337-G-T

http://identifiers.org/hco/7/GRCh38#45720789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7126370-C-A

45721196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7126693-G-A

45721196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7126693-G-T

45721279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7126776-C-T

http://identifiers.org/hco/7/GRCh38#45721355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7126848-C-A

45721355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7126848-C-G

45721399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7126885-C-T

45721612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7127031-T-C

45721703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7127095-A-G

http://identifiers.org/hco/7/GRCh38#45721848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7127251-A-C

45721848-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7127251-A-T

45721849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7127252-G-A

http://identifiers.org/hco/7/GRCh38#45722001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7127395-C-A

45722001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7127395-C-T

http://identifiers.org/hco/7/GRCh38#45722172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7127569-C-A

45722216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7127633-G-A

45722216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7127633-G-C

45722431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7127860-G-A

45722431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7127860-G-T

45722463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7127869-G-A

http://identifiers.org/hco/7/GRCh38#45722549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7127954-C-A

45722549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7127954-C-T

45722684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7128095-T-C

45722760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7128169-G-A

45722760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7128169-G-T

http://identifiers.org/hco/7/GRCh38#45722879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#7128278-C-A

45722879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 232
most severe consequence: 3 prime UTR variant
orthologous variants: 7128278-C-T