http://identifiers.org/hco/2/GRCh38#127701378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32044438-C-A

127701378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32044438-C-G

127701378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32044438-C-T

http://identifiers.org/hco/2/GRCh38#127701453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32044372-C-A

127701453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32044372-C-T

127701459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32044366-G-A

127701459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32044366-G-C

127701459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32044366-G-T

http://identifiers.org/hco/2/GRCh38#127701466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32044359-C-A

127701466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32044359-C-T

127701488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32044325-G-A

127701488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32044325-G-C

127701488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32044325-G-T

127701492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32044319-G-A

127701492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32044319-G-T

127701511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 32044308-G-A

127701511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 32044308-G-C

127701511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 32044308-G-T

http://identifiers.org/hco/2/GRCh38#127701512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32044307-C-A

127701512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 32044307-C-G

127701512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 32044307-C-T

127701532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32044286-G-A

127701532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32044286-G-C

127701532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32044286-G-T

http://identifiers.org/hco/2/GRCh38#127701553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32044265-C-A

127701553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32044265-C-G

127701553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: 32044265-C-T

127701669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32044158-G-A

127701669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32044158-G-C

127701669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32044158-G-T

127701700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32044127-G-A

127701700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32044127-G-C

127701700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32044127-G-T

127701709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32044118-G-A

127701709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32044118-G-T

http://identifiers.org/hco/2/GRCh38#127701720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32044107-C-A

127701720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32044107-C-T

127701758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32044069-T-C

127701841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043986-G-A

127701841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043986-G-C

127701841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043986-G-T

127701889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043938-G-A

127701889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043938-G-C

127701889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043938-G-T

http://identifiers.org/hco/2/GRCh38#127701899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32043928-C-A

127701899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043928-C-T

http://identifiers.org/hco/2/GRCh38#127701928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32043899-C-A

127701928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043899-C-T

http://identifiers.org/hco/2/GRCh38#127701934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32043893-C-A

127701934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043893-C-G

127701934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32043893-C-T

http://identifiers.org/hco/2/GRCh38#127701967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32043860-C-A

127701967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043860-C-G

127701967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32043860-C-T

127702033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043794-A-G

127702033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043794-A-T

http://identifiers.org/hco/2/GRCh38#127702039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32043788-C-A

127702039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043788-C-G

127702039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32043788-C-T

127702057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043770-G-A

127702057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043770-G-C

127702057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043770-G-T

http://identifiers.org/hco/2/GRCh38#127702074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32043753-C-A

127702074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32043753-C-G

127702074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32043753-C-T

127702081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043746-G-A

127702081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043746-G-T

127702083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32043744-T-A

127702083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32043744-T-C

127702147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043680-G-A

127702147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043680-G-C

127702147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043680-G-T

http://identifiers.org/hco/2/GRCh38#127702153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32043674-C-A

127702153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32043674-C-T

http://identifiers.org/hco/2/GRCh38#127702158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32043669-C-A

127702158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32043669-C-T

http://identifiers.org/hco/2/GRCh38#127702261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32043601-C-A

127702261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32043601-C-G

127702261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32043601-C-T

127702444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32043423-G-A

127702444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32043423-G-C

127702447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32043420-T-A

127702527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32043327-T-C

http://identifiers.org/hco/2/GRCh38#127702555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32043307-C-A

127702558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32043304-T-C

127702586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32043271-G-A

http://identifiers.org/hco/2/GRCh38#127702944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32042956-C-A

127703060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32042837-T-G

http://identifiers.org/hco/2/GRCh38#127703263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32042663-C-A

127703263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32042663-C-T

127704115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32042307-T-C

127704251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32042179-G-A

127704280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32042150-A-G

http://identifiers.org/hco/2/GRCh38#127705392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32040911-C-A

127705409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32040896-G-A

127705561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32040783-G-A

127705563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32040781-G-T

127705647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32040704-T-C

127705668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32040685-G-A

127705845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32040523-G-A

127705911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32040459-T-C

http://identifiers.org/hco/2/GRCh38#127706098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32040276-C-A

127706165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: 32040200-T-C

http://identifiers.org/hco/2/GRCh38#127706170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32040195-C-A

http://identifiers.org/hco/2/GRCh38#127706299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32040066-C-A

http://identifiers.org/hco/2/GRCh38#127706303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32040062-A-C

127706414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32039955-C-G

127706474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 32039895-C-T

http://identifiers.org/hco/2/GRCh38#127706645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32039721-A-C

127706645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32039721-A-G

127706653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32039716-T-A

127706653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32039716-T-C

127706673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32039696-G-A

127708358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32037778-G-A

127708531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32037645-G-T

127708649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32037527-G-A

127708657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32037519-A-G

127708757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32037422-G-A

http://identifiers.org/hco/2/GRCh38#127708928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32037225-C-A

127708928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32037225-C-G

127708928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32037225-C-T

127708951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32037202-A-G

127709038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32037126-G-T

http://identifiers.org/hco/2/GRCh38#127709041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32037123-A-C

127709041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32037123-A-G

127709043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32037121-C-T

127709336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32035855-G-A

http://identifiers.org/hco/2/GRCh38#127709436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32035772-C-A

127709579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32035636-C-T

127709665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32035564-G-A

127709714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: stop_gained, synonymous_variant
orthologous variants: 32035517-G-A

127709714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 32035517-G-C

http://identifiers.org/hco/2/GRCh38#127709716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32035515-C-A

127709716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32035515-C-T

127709755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32035476-T-C

http://identifiers.org/hco/2/GRCh38#127709795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32035436-A-C

127709815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32035416-G-A

127709839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32035392-G-A

127709842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32035389-G-A

127709861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32035370-A-G

127709861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32035370-A-T

http://identifiers.org/hco/2/GRCh38#127709882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32035353-C-A

http://identifiers.org/hco/2/GRCh38#127709914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32035331-C-A

127709914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32035331-C-T

http://identifiers.org/hco/2/GRCh38#127709915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32035330-A-C

127709915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32035330-A-G

127709928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32035317-G-A

127709928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32035317-G-T

127711161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32031058-A-G

127711181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32031039-T-C

127711495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32030666-G-A

127713107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32030546-A-G

127713278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32030397-C-G

127713278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32030397-C-T

127713286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32030389-T-A

127713286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32030389-T-G

127713434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32030215-A-T

127713476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32030174-T-G

127713495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32030155-C-T

127713553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32030118-T-A

127713553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32030118-T-C

127713607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron_variant, missense_variant
orthologous variants: 32030063-C-T

127713796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron_variant, missense_variant
orthologous variants: 32029874-A-G

127714142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32029533-T-G

http://identifiers.org/hco/2/GRCh38#127714146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32029529-C-A

127715565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32028057-A-G

127716234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32026997-C-G

127716234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32026997-C-T

127716288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32026953-A-T

127716357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32026884-A-G

http://identifiers.org/hco/2/GRCh38#127716362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32026879-A-C

127717048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32026250-G-A

127717048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32026250-G-T

127717106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32026197-C-T

127717291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32026014-A-G

127717291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32026014-A-T

127717367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32025938-T-C

127719039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32022413-T-C

127719134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32022318-A-G

127719144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32022308-A-T

http://identifiers.org/hco/2/GRCh38#127719189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32022265-C-A

127719189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32022265-C-T

http://identifiers.org/hco/2/GRCh38#127719233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32022227-C-A

127719317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32022139-T-C

127719509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32021947-G-A

127719663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32021793-G-A

127719758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32021713-T-C

127719758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32021713-T-G

127719788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32021683-G-A

127719788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32021683-G-C

http://identifiers.org/hco/2/GRCh38#127720250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32021224-C-A

127720286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32021188-G-A

127720402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32021064-C-G

127721921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32020815-A-G

127722008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32020726-T-C

127722068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron_variant, undefined
orthologous variants: 32020672-T-G

http://identifiers.org/hco/2/GRCh38#127722084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32020662-A-C

http://identifiers.org/hco/2/GRCh38#127722086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32020660-C-A

127722086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32020660-C-T

127722337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32020271-G-A

127722395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32020216-G-T

127722592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 32019844-T-C

127722756-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32019680-G-C

http://identifiers.org/hco/2/GRCh38#127722856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32019575-C-A

127723075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32019040-A-G

http://identifiers.org/hco/2/GRCh38#127723092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32019026-C-A

127723092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32019026-C-G

127723092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32019026-C-T

127723185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32018585-C-T

127723203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32018569-T-C

http://identifiers.org/hco/2/GRCh38#127723242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32018530-A-C

http://identifiers.org/hco/2/GRCh38#127723264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32018510-C-A

127723303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32018471-C-T

http://identifiers.org/hco/2/GRCh38#127723364-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32018407-A-C

127723476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32018317-T-A

127724466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32014190-A-G

127724736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32013935-T-A

127724736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32013935-T-C

127724742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32013930-G-C

127724742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32013930-G-T

http://identifiers.org/hco/2/GRCh38#127724869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32013088-C-A

127724869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32013088-C-G

127725011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32012949-G-A

127725021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32012927-G-A

127725021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32012927-G-C

127725204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32012733-T-C

127725237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32012699-A-G

http://identifiers.org/hco/2/GRCh38#127725294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32012640-A-C

127725316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32012618-T-C

http://identifiers.org/hco/2/GRCh38#127725321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32012613-C-A

127725475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32012518-G-A

127725523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32012487-G-A

127725526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32012484-C-G

127726270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32011553-G-A

127726343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32011481-C-T

127726486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32011361-A-G

127726596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32011258-C-T

127726774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: missense variant
orthologous variants: 32011078-T-C

127726818-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32011035-T-A

127726818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32011035-T-C

127726818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32011035-T-G

127727171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32010746-C-T

127727806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: -C-T

127727932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: -G-A

127728031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: -A-G

127728031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: -A-T

127728067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: -T-C

127728151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: -C-T

127728416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: -A-G

127728435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: -G-C

127728435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: -G-T

127728470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: -C-T

127728479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: -T-A

127728487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: -C-G

127728487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: -C-T

127730895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32005149-G-A

127731082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32005048-C-T

127733421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32004515-A-G

127733421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32004515-A-T

127734272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32004105-G-T

127734295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32004077-G-A

127734416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32003970-G-A

127734416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32003970-G-C

http://identifiers.org/hco/2/GRCh38#127735299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32002717-C-A

127735299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32002717-C-T

127735302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32002714-A-T

127735340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32002677-T-C

127735340-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32002677-T-G

127735343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 32002674-G-T

127735411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32002610-G-A

127735411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32002610-G-C

127735626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32002397-C-T

127735866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32002174-G-T

http://identifiers.org/hco/2/GRCh38#127735910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32002145-A-C

127735910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32002145-A-G

127735927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32002128-G-C

http://identifiers.org/hco/2/GRCh38#127736498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#32001643-A-C

127736875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32001283-T-A

127737005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32001182-G-A

127737005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32001182-G-T

127737217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32001019-A-T

127737223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32001013-T-A

127737256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32000977-G-C

127737343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32000895-T-C

127737343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32000895-T-G

127737348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32000890-G-C

127737381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32000857-G-A

127737381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32000857-G-C

127737413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 32000830-T-C

127740217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31998465-C-G

127740217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31998465-C-T

127740257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31998426-G-A

127744679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31992639-G-A

127745107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31992290-T-A

127745152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31992245-G-C

127745168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31992229-T-C

127745829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31990947-C-T

127745844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31990927-T-C

127745884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31990885-G-A

http://identifiers.org/hco/2/GRCh38#127746092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31990718-C-A

127746092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31990718-C-T

127746114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31990682-T-C

127746132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31990664-G-A

127746141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31990655-A-G

127746151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31990645-G-A

127746256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31990506-C-G

http://identifiers.org/hco/2/GRCh38#127746274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31990487-A-C

127746330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31990432-C-T

127746569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31990232-C-T

127746596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31990194-G-A

127746596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31990194-G-C

http://identifiers.org/hco/2/GRCh38#127746612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31990127-C-A

127753594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31979191-A-G

127753628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31979157-T-C

127758679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31971934-T-A

127758679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31971934-T-C

127759892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31971543-T-A

127759956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31971480-T-C

http://identifiers.org/hco/2/GRCh38#127760236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31971096-A-C

127760334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31971003-A-G

127762059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31969427-A-G

127762211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31969277-C-T

127762631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31968924-A-G

http://identifiers.org/hco/2/GRCh38#127762674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31968880-C-A

127762674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31968880-C-G

127762674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31968880-C-T

127762947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31968646-G-A

127762947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31968646-G-C

127762947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31968646-G-T

http://identifiers.org/hco/2/GRCh38#127763440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31968159-C-A

127763575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31968023-C-T

127763643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31967948-T-C

127763661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31967930-T-C

127763704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31967883-A-G

http://identifiers.org/hco/2/GRCh38#127763903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31967702-C-A

127763903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31967702-C-T

http://identifiers.org/hco/2/GRCh38#127764096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31967521-C-A

127764203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31967420-G-A

127764203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 31967420-G-T

127765745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31965118-G-A

127765745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31965118-G-T

http://identifiers.org/hco/2/GRCh38#127766261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31964873-C-A

127767744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31963593-A-G

127767977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31963374-C-T

127768087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31963266-A-T

http://identifiers.org/hco/2/GRCh38#127768097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31963256-A-C

127768097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31963256-A-T

127768123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31963094-T-C

127768395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31962819-G-A

127768395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31962819-G-T

127768820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31962455-T-C

127768820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31962455-T-G

127768872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31962410-A-G

127768872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31962410-A-T

127769766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31961152-T-C

127769967-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31961017-T-G

127769971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31961013-G-A

127770304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31960862-A-T

127770758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31960559-A-G

127770806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron_variant, missense_variant
orthologous variants: 31960511-T-C

http://identifiers.org/hco/2/GRCh38#127771080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31960228-C-A

127776994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31956267-C-G

127776994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31956267-C-T

127777397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31955882-A-G

127808332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31940346-C-G

127808332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31940346-C-T

127809057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31939811-T-A

127809057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31939811-T-C

127809456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31939355-G-A

127809456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31939355-G-T

127809697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31939230-A-G

127809815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31939095-T-C

127809815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31939095-T-G

127810224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31938750-G-C

http://identifiers.org/hco/2/GRCh38#127810613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31937643-C-A

127810613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31937643-C-T

http://identifiers.org/hco/2/GRCh38#127810728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31937536-C-A

127810728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: 31937536-C-T

http://identifiers.org/hco/2/GRCh38#127810739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31937528-C-A

http://identifiers.org/hco/2/GRCh38#127810837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31937462-C-A

127810837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31937462-C-G

http://identifiers.org/hco/2/GRCh38#127810849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31937450-A-C

127810849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31937450-A-G

127810849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31937450-A-T

http://identifiers.org/hco/2/GRCh38#127810857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#31937442-C-A

127810857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 31937442-C-T

http://identifiers.org/hco/2/GRCh38#127810971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#31937342-C-A

127810971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31937342-C-T

127810995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31937323-G-A

127810995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 31937323-G-T

http://identifiers.org/hco/2/GRCh38#127811043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#31937275-C-A

127811043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 31937275-C-T

127811082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25651
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 31937236-T-C