2475242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24424388-C-T

2475702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24423964-G-T

2475816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24423878-T-C

2476218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24423557-G-C

2476353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24423492-G-C

http://identifiers.org/hco/16/GRCh38#2476366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24423479-C-A

http://identifiers.org/hco/16/GRCh38#2476542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24423300-C-A

2476542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24423300-C-G

http://identifiers.org/hco/16/GRCh38#2476622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24423238-C-A

2476622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24423238-C-T

2476713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24423147-T-A

2478344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24422112-G-T

2478502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24421970-T-C

http://identifiers.org/hco/16/GRCh38#2481099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24420136-C-A

2481099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24420136-C-T

2481188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24420039-T-C

2481491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24419915-G-A

2481547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24419852-G-A

2481547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24419852-G-T

2481564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24419830-T-C

http://identifiers.org/hco/16/GRCh38#2481773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24419678-C-A

http://identifiers.org/hco/16/GRCh38#2481844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24419628-C-A

2481844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24419628-C-T

2481915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24419557-A-G

http://identifiers.org/hco/16/GRCh38#2481935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24419537-C-A

2481935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24419537-C-G

http://identifiers.org/hco/16/GRCh38#2481987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24419484-C-A

2482048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24419419-G-C

2482087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24419403-G-A

2482106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24419386-G-C

2482207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24419316-T-C

2482246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24419276-A-G

2482246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24419276-A-T

2482340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24419186-G-A

2482398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24419150-C-T

2482719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418877-G-A

2482858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418744-G-T

2482881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418716-G-A

2482881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418716-G-T

2482887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418710-T-A

2482887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418710-T-C

2482887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418710-T-G

2482900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418702-G-A

2482900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418702-G-C

2482900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418702-G-T

2482918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418684-G-A

2482931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418673-T-C

2482939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418665-G-A

2482939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24418665-G-T

2483049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418595-A-G

2483050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418594-G-A

2483050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418594-G-T

http://identifiers.org/hco/16/GRCh38#2483162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24418476-C-A

2483162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418476-C-T

http://identifiers.org/hco/16/GRCh38#2483165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24418473-C-A

2483167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418471-T-C

2483188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418454-G-A

2483188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418454-G-T

2483195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418447-G-A

2483195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418447-G-T

2483242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418392-A-G

2483440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418188-A-G

2483490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418130-A-G

2483490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418130-A-T

2483522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418065-G-A

2483522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24418065-G-T

http://identifiers.org/hco/16/GRCh38#2483585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24417957-C-A

2483585-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24417957-C-G

2483694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24417830-G-T

2483799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24417752-T-C

2483838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24417708-A-G

2483838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24417708-A-T

2483883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24417671-G-A

2483887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24417667-G-T

http://identifiers.org/hco/16/GRCh38#2484104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24417518-C-A

http://identifiers.org/hco/16/GRCh38#2484394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24417243-C-A

2484394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24417243-C-T

2484401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24417236-C-T

http://identifiers.org/hco/16/GRCh38#2484430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24417201-C-A

2484430-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24417201-C-G

http://identifiers.org/hco/16/GRCh38#2484503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24417166-C-A

2484503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24417166-C-T

http://identifiers.org/hco/16/GRCh38#2484519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24417149-C-A

2484544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24417125-C-T

2484618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24417071-A-G

http://identifiers.org/hco/16/GRCh38#2484704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24417000-C-A

2484704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24417000-C-T

http://identifiers.org/hco/16/GRCh38#2484772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24416946-C-A

2484805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24416907-T-C

http://identifiers.org/hco/16/GRCh38#2484944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#24416819-C-A

2484944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24416819-C-T

2486995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24415730-A-G

2487095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24415654-C-G

2487182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24415601-C-T

http://identifiers.org/hco/16/GRCh38#2490046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24413453-C-A

2490046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24413453-C-T

2490083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24413402-T-C

2490228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24413252-T-C

http://identifiers.org/hco/16/GRCh38#2490600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24412955-A-C

2491253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24411956-T-G

2492541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24411147-T-A

2492616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24411089-T-C

http://identifiers.org/hco/16/GRCh38#2492698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24411014-C-A

2492722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24410996-G-A

2493714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 24408908-T-C

2493731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24408891-C-T

2493814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24407156-A-G

2493847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24407124-C-T

2494027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24406928-G-A

2494027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24406928-G-C

2494280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24405860-C-G

2494280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24405860-C-T

2494311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24405830-C-T

2494312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24405829-T-A

2494312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24405829-T-C

2494815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24405401-C-T

2495934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24405348-T-A

2495934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24405348-T-C

2496014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24405277-G-T

http://identifiers.org/hco/16/GRCh38#2496067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24405224-C-A

2496067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24405224-C-T

2496161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24405128-G-C

2496299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24404990-C-T

2496308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24404981-G-T

2496462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24404827-G-A

2496617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 24404672-C-T

2497241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24403776-T-C

http://identifiers.org/hco/16/GRCh38#2497253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24403764-C-A

2497253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24403764-C-G

http://identifiers.org/hco/16/GRCh38#2497259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24403756-A-C

2497741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 24403339-T-C

http://identifiers.org/hco/16/GRCh38#2497758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24403315-C-A

2498257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 24402805-G-A

2498257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 24402805-G-T

2498469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24402592-G-A

2498469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24402592-G-T

2498493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24402568-G-A

2498493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24402568-G-T

2498503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24402558-T-C

2498539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24402519-T-C

2498540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24402518-G-A

2498540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24402518-G-T

2498695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24402362-G-A

2498710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24402348-G-A

2498716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24402342-C-T

2499027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24402066-C-T

http://identifiers.org/hco/16/GRCh38#2499306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24401871-C-A

2499306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24401871-C-T

2499340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24401840-G-C

2499692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24401652-A-T

2499816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24401535-A-G

2499969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24401309-C-T

http://identifiers.org/hco/16/GRCh38#2500082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24401140-C-A

2500082-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24401140-C-G

2500082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24401140-C-T

http://identifiers.org/hco/16/GRCh38#2500233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24400995-C-A

2500233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24400995-C-G

http://identifiers.org/hco/16/GRCh38#2500261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24400963-A-C

2500261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 24400963-A-G

http://identifiers.org/hco/16/GRCh38#2500357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24400867-C-A

2500357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 24400867-C-T

http://identifiers.org/hco/16/GRCh38#2500388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24400830-C-A

2500388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 24400830-C-T

2500439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 24400779-T-A

2500469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 24400749-G-A

2500469-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 24400749-G-C

2500469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 24400749-G-T

2500529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24400674-G-T

2500532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24400671-T-A

2500643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 24400531-G-A

http://identifiers.org/hco/16/GRCh38#2500726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24400436-C-A

2500951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 24400220-C-G

2501083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24400071-A-G

2501127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24400050-G-T

http://identifiers.org/hco/16/GRCh38#2501190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24400002-C-A

2501190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24400002-C-G

2501190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24400002-C-T

http://identifiers.org/hco/16/GRCh38#2501202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24399990-C-A

2501202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24399990-C-G

2501591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24399784-C-T

2501616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 24399751-G-T

2501759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24399601-A-G

http://identifiers.org/hco/16/GRCh38#2501763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24399597-C-A

2501763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24399597-C-T

2501808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24399553-T-A

2501808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24399553-T-C

http://identifiers.org/hco/16/GRCh38#2502019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24399375-C-A

2502019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24399375-C-T

http://identifiers.org/hco/16/GRCh38#2502035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24399361-C-A

2502035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24399361-C-T

2502098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24399315-G-C

2502098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24399315-G-T

2502142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24399270-T-A

2502142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24399270-T-C

http://identifiers.org/hco/16/GRCh38#2502143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24399269-C-A

2502177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24399231-C-T

2502190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24399218-G-T

http://identifiers.org/hco/16/GRCh38#2502260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24398999-C-A

2502286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398976-A-G

2502304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398958-T-C

http://identifiers.org/hco/16/GRCh38#2502356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24398907-C-A

2502356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398907-C-T

2502358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398905-G-A

2502358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398905-G-T

2502393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398870-G-A

2502443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398839-G-A

2502443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398839-G-T

http://identifiers.org/hco/16/GRCh38#2502482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24398801-C-A

2502482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398801-C-T

http://identifiers.org/hco/16/GRCh38#2502498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24398785-C-A

2502498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398785-C-T

2502651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398657-G-A

2502651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398657-G-T

2502662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398646-T-A

http://identifiers.org/hco/16/GRCh38#2502699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24398620-C-A

2502699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398620-C-T

http://identifiers.org/hco/16/GRCh38#2502781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24398556-C-A

2502781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24398556-C-T

2503027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 24398191-G-A

2503027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, undefined
orthologous variants: 24398191-G-T

http://identifiers.org/hco/16/GRCh38#2503187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24398073-C-A

2503493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24397842-A-G

2503494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24397841-A-T

2503544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24397797-G-A

2503544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24397797-G-T

2503697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24397714-A-G

2503705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24397706-G-A

2503705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24397706-G-C

2503705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24397706-G-T

http://identifiers.org/hco/16/GRCh38#2503808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24397572-C-A

2503808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24397572-C-G

2503808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24397572-C-T

2503828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 24397554-G-T

http://identifiers.org/hco/16/GRCh38#2507063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#24393812-C-A

2507063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24393812-C-T

2507066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24393808-C-T

2507075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: non coding transcript exon variant
orthologous variants: 24393799-T-C

http://identifiers.org/hco/16/GRCh38#2507239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24393647-C-A

2507392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24393485-A-G

2507551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: non coding transcript exon variant
orthologous variants: 24393385-C-G

2507561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: non coding transcript exon variant
orthologous variants: 24393375-T-C

http://identifiers.org/hco/16/GRCh38#2507643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24393324-C-A

2507643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: non coding transcript exon variant
orthologous variants: 24393324-C-T

2507712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: non coding transcript exon variant
orthologous variants: 24393296-T-A

2507712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: non coding transcript exon variant
orthologous variants: 24393296-T-C

2507788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29203
most severe consequence: non coding transcript exon variant
orthologous variants: 24393212-G-T