http://identifiers.org/hco/6/GRCh38#150599999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3690447-C-A

150599999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 3690447-C-G

150599999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 3690447-C-T

150600027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690474-G-A

150600027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690474-G-T

150600048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690478-G-A

150600048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690478-G-C

150600048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690478-G-T

http://identifiers.org/hco/6/GRCh38#150600051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3690481-C-A

150600051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690481-C-T

150600078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690509-G-A

150600078-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690509-G-C

150600078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690509-G-T

http://identifiers.org/hco/6/GRCh38#150600097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3690528-C-A

150600097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690528-C-T

150600113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690544-G-A

150600113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690544-G-T

150600204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690607-G-A

150600209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690612-C-T

150600213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3690616-G-C

150600813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3691180-G-A

150600813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3691180-G-C

150600813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3691180-G-T

http://identifiers.org/hco/6/GRCh38#150600824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3691193-C-A

150600831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3691200-T-G

150600867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 3691235-C-T

http://identifiers.org/hco/6/GRCh38#150600936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#3691328-C-A

150600936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3691328-C-T

http://identifiers.org/hco/6/GRCh38#150600976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#3691365-C-A

150600976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3691365-C-T

http://identifiers.org/hco/6/GRCh38#150601934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3692347-C-A

150601990-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3692523-C-G

150602092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3692628-A-G

150602092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3692628-A-T

http://identifiers.org/hco/6/GRCh38#150602422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3692946-A-C

http://identifiers.org/hco/6/GRCh38#150602441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3692965-C-A

150602441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3692965-C-T

150602468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3692992-A-T

http://identifiers.org/hco/6/GRCh38#150602580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3693121-C-A

150602674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3693238-G-A

150602822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3693365-G-A

http://identifiers.org/hco/6/GRCh38#150603139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3693743-C-A

150603278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3693902-C-T

150603321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3693948-C-G

150603754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3694310-C-T

http://identifiers.org/hco/6/GRCh38#150604152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3695268-A-C

150604152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3695268-A-G

150604210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3695315-A-G

150604234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3695339-C-T

150605544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3696044-A-G

150605581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3696093-G-T

150605634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3696144-G-A

150605634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3696144-G-T

150605707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3696209-T-A

150605707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3696209-T-C

150605895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3696420-G-A

http://identifiers.org/hco/6/GRCh38#150605968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3696472-C-A

150605968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3696472-C-G

150606188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3696678-C-T

150606389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3696879-G-A

150606442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3696934-G-A

150606442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3696934-G-T

150606729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3697179-G-T

http://identifiers.org/hco/6/GRCh38#150606958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3697341-A-C

150607257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3697599-A-G

150607317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3697651-G-A

http://identifiers.org/hco/6/GRCh38#150607501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3697818-C-A

150607501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3697818-C-T

150607656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3697983-T-G

150607674-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3697999-A-T

150607804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698101-G-C

150607808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698105-G-A

150607897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698194-G-A

150607955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698248-A-T

150607957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698250-C-T

150608017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698327-G-C

150608056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698366-T-C

150608137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698410-A-G

150608144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698417-T-A

150608429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3698694-A-G

150608479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3699186-C-T

150608721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3699380-G-A

150608724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3699383-A-T

150609300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3700021-G-A

150609333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3700055-G-T

http://identifiers.org/hco/6/GRCh38#150609453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3700854-C-A

150609486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3700889-A-G

150609565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3700968-G-T

150609612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701014-G-A

150609616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701018-G-A

150609779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701162-G-A

150609823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701205-C-T

150609855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701232-C-G

150609855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701232-C-T

150609856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701233-G-A

150609856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701233-G-C

150609925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701294-C-T

150609969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701346-A-G

150609971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701348-G-A

150610199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701545-T-G

150610204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701550-C-T

150610205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701551-G-A

150610228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701558-A-G

150610314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701643-C-T

150610327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701653-C-T

150610412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3701816-C-G

150610650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3702072-G-A

150610672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3702094-G-A

150610885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3703165-C-G

150610885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3703165-C-T

150611090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3703379-C-T

150611142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3703419-T-A

150611753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3703759-A-G

http://identifiers.org/hco/6/GRCh38#150611768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3703774-C-A

150611938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3703879-G-T

http://identifiers.org/hco/6/GRCh38#150611984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3703957-C-A

http://identifiers.org/hco/6/GRCh38#150612051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#3704006-C-A

150612051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3704006-C-G

150612051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3704006-C-T

http://identifiers.org/hco/6/GRCh38#150612052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#3704007-C-A

150612052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3704007-C-G

150612052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3704007-C-T

http://identifiers.org/hco/6/GRCh38#150612084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3704038-A-C

150612200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3704149-C-G

150612579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3704467-C-T

150612623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3704508-A-T

http://identifiers.org/hco/6/GRCh38#150612650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3704530-A-C

http://identifiers.org/hco/6/GRCh38#150612653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3704533-C-A

150612653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3704533-C-T

150612935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3704714-C-T

150613250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3704933-T-C

150613301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3704983-G-A

150613301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3704983-G-T

150613354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3705036-C-T

150613464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3705169-C-T

150613473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3705178-C-T

150613494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3705204-C-T

150613579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3705392-C-T

150613632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3705476-C-T

150614033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3706624-A-G

http://identifiers.org/hco/6/GRCh38#150614068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3706662-A-C

150614114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3706692-T-A

150616012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3706838-G-T

150616023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3706858-G-A

150616294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3707105-G-A

150616294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3707105-G-C

150616475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3707277-G-T

150616617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3707399-A-G

150616763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3707510-G-A

150616763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3707510-G-C

150616787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3707531-C-T

150616795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3707537-T-C

150616912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3707662-C-T

150616922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3707672-T-C

150616959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3707709-G-A

150617266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3707985-C-T

http://identifiers.org/hco/6/GRCh38#150617358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3708075-C-A

150617358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3708075-C-G

150617358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3708075-C-T

150617468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3708176-C-G

150617760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3708468-G-A

150617964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3708643-G-A

150618067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3708745-T-C

150618116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3708797-G-A

150622061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3711310-G-T

150622066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3711315-G-A

150622193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3711424-A-G

150622487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3711734-C-T

150622587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3711815-A-G

150622635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3711852-A-G

150622839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3712067-T-C

150623077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3712256-C-T

150623347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3712553-G-A

150624464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3715071-T-A

150624465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3715072-G-T

150624546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3715139-G-A

150624546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3715139-G-T

150624609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3715197-T-C

150624654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3715242-T-C

http://identifiers.org/hco/6/GRCh38#150624707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3715286-C-A

150624707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3715286-C-T

150625894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3716863-G-A

150625894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3716863-G-T

http://identifiers.org/hco/6/GRCh38#150625902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3716871-C-A

150625954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3716945-G-A

150625988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3716979-G-T

http://identifiers.org/hco/6/GRCh38#150626061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3717051-C-A

http://identifiers.org/hco/6/GRCh38#150626066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3717056-C-A

150626307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3717226-A-G

150626343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3717262-A-G

150626464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3717377-G-A

150626539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3717443-G-A

150626636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3717538-A-G

150626857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3717732-C-T

150626937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3717809-C-T

150627459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3718321-C-T

150627792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3719660-G-C

http://identifiers.org/hco/6/GRCh38#150627802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3719670-C-A

150628347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3720227-A-G

150628611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3720478-A-G

150629018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3720931-T-G

150629019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3720932-C-T

150629301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3721192-G-A

150629783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3721399-A-G

150629832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3721428-G-A

150629916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3721536-G-A

150629954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3721574-G-A

150629985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3721605-A-G

150630027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3721646-C-T

150630036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3721655-A-G

150630287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3721847-A-G

150630480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3722021-A-G

150630881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3722443-G-C

150630881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3722443-G-T

150630904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3722473-G-A

150631275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3722935-G-A

150631550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3723594-G-A

150631662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3723674-T-G

150631745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3723748-G-A

150631745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3723748-G-T

150631783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3724175-G-A

150632033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3724461-T-G

150632338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3724807-T-A

150632496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3724970-G-A

150632521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3725034-G-A

150632554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3725092-C-T

150632634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3725193-G-A

150632762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3732681-A-T

150632772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3732691-A-T

150632909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3733092-G-T

http://identifiers.org/hco/6/GRCh38#150632927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3733115-C-A

http://identifiers.org/hco/6/GRCh38#150632944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3733132-A-C

150632979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3733165-A-G

http://identifiers.org/hco/6/GRCh38#150633167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3733347-C-A

150633167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3733347-C-T

150633207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3733387-G-A

150633215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3733395-T-C

150633229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3733406-G-A

150633229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3733406-G-T

150633243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3733427-G-A

150633243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3733427-G-T

150633275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3733456-T-C

http://identifiers.org/hco/6/GRCh38#150633387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3733537-C-A

150633387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3733537-C-T

150633388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3733538-A-G

150633396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3733543-T-C

http://identifiers.org/hco/6/GRCh38#150633420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3733566-C-A

150633420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3733566-C-T

150633422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3733568-T-C

150633422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3733568-T-G

150633433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3733579-A-G

150633440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3733586-T-C

150633472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3733618-G-A

150633559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3733703-G-A

150634807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3735301-C-T

150634863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3735353-G-T

http://identifiers.org/hco/6/GRCh38#150634968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3735456-C-A

150635047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3735534-A-G

150635278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3735767-A-G

150635588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3736752-A-G

150635619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3736781-G-T

http://identifiers.org/hco/6/GRCh38#150635690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3736862-A-C

150635945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3737091-A-G

150635983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3737125-T-C

150635984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3737126-G-T

150636281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3737415-A-T

150636377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3737477-G-A

150636389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3737489-A-G

150636830-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3737874-T-G

150637421-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3738382-A-T

150637533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3738487-G-A

150637603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3738576-C-T

150637659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3738640-A-G

150638177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3739265-C-T

http://identifiers.org/hco/6/GRCh38#150638181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3739269-A-C

150638181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3739269-A-G

150638322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3739406-G-A

http://identifiers.org/hco/6/GRCh38#150638652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3739708-C-A

150638652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3739708-C-T

150638845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3739873-A-G

150638874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3739902-T-C

150638874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3739902-T-G

150641292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3741195-C-G

150641316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3741220-C-T

150641342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3741246-C-T

150641362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3741266-G-A

150641543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3741446-A-G

150641648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3741551-T-C

150641649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3741552-G-A

http://identifiers.org/hco/6/GRCh38#150641725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3741628-C-A

150641865-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3741749-A-T

http://identifiers.org/hco/6/GRCh38#150641915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3741790-C-A

150641915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3741790-C-T

150641947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3741821-G-A

150641947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3741821-G-T

150642050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3741911-G-T

150642103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3741965-A-G

150642168-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3742016-T-G

150642279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3742729-T-G

150642291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3742739-T-C

150642391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3742837-G-A

150642441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3742883-T-A

150642536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3742975-A-G

150642571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3743007-A-G

150642674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3743113-G-A

150643093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3743437-T-C

150643455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3743760-T-A

150643455-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3743760-T-G

150643670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3743991-A-T

150643811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3744132-A-T

150644272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3744595-T-C

http://identifiers.org/hco/6/GRCh38#150646790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3746981-C-A

150646968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3748730-A-G

150647444-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3749167-T-G

150647492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3749221-C-T

150647526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3749251-C-G

150647733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3749473-A-G

150648231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3749981-A-G

150648523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3750454-A-G

150648535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3750465-T-C

150648560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3750486-A-G

150648804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3750707-G-T

http://identifiers.org/hco/6/GRCh38#150648866-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3750768-A-C

150648873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3750775-T-A

150649256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3751163-T-G

150649445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3751277-T-C

150649457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3751289-C-T

150649492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3751319-A-T

150650037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3751695-G-A

150650301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3751908-A-G

150650586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3752154-G-A

150652808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3753758-A-T

150653379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3754309-C-G

150653838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3754805-C-T

150653889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3754855-G-A

150654684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3756738-T-C

150654752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3756805-T-C

150654839-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3756891-C-G

150655038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3757092-T-A

150655095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3757150-G-A

150656244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3757294-C-T

150656346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3757635-C-T

150656789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3757972-G-T

150656843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3758004-A-T

150657220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3758338-T-G

http://identifiers.org/hco/6/GRCh38#150657503-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3758715-A-C

150657621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3758820-C-T

150657629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3758828-T-C

150657803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3758997-A-G

150657842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3759035-C-T

150657852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3759045-A-G

150657854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3759046-A-G

150658317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3759528-C-G

150658394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3759603-G-A

150658404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3759613-G-C

http://identifiers.org/hco/6/GRCh38#150658632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3759872-A-C

150658632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3759872-A-G

150658819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3760034-C-G

150658819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3760034-C-T

150658830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3760076-T-C

150658856-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3760119-G-C

150659341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3760901-A-T

150659395-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3760971-G-C

150659587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3761155-G-A

150659587-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3761155-G-C

150660450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3761956-C-T

150660826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3762271-A-G

150661035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3762477-G-A

150661035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3762477-G-C

150661035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3762477-G-T

150661422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3762934-T-G

150661436-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3762946-T-A

150661563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3763056-G-T

150661566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3763059-C-T

150661861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3763337-A-G

150661927-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3763413-C-G

150662711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3764621-C-T

150662730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3764640-G-A

150662730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3764640-G-T

150662734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3764644-G-A

150662734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3764644-G-T

150662757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3764664-T-C

150662768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3764675-T-C

150662794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3764702-G-A

150662809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3764722-C-T

150663061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3764943-A-G

http://identifiers.org/hco/6/GRCh38#150663287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3765169-C-A

150663341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3765574-G-A

150663483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3766323-T-C

150663500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3766340-A-G

150663512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3766351-C-G

150664051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3766421-G-T

150664135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3766499-A-G

150664296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3766638-G-T

150664451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 3766762-A-G

150664545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3766857-G-A

http://identifiers.org/hco/6/GRCh38#150664623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3766912-C-A

150664798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3767088-G-T

150664853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3767140-G-A

150665091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3767337-A-G

150665178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3767435-A-G

150665333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3767590-T-C

150665354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3767611-A-G

150668255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3769256-C-T

150668383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3769328-G-T

150668389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3769334-C-T

150668476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3769417-A-T

150668733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3769672-C-T

150669291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3770190-G-T

150669476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3770373-G-A

150670521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3771205-A-G

150670580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3771263-T-C

150670698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3771381-G-A

150671930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3771948-T-G

150673026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3774057-T-A

150673096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3774127-A-G

150673437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3774450-G-A

150673556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3774547-A-G

150674002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3775270-G-C

150674126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3775366-C-T

150674303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3775557-A-G

150674397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3775650-G-T

150674429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3775680-T-G

150674607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3775876-C-T

150675148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3776043-C-T

150675288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3776201-G-T

150675328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3776239-C-T

150679258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3778251-G-A

150679258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3778251-G-T

150679474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3778563-C-T

150679515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3778603-C-T

150679659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3778756-A-G

150679661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3778758-G-A

150681713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3780266-G-A

150682051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3780610-G-A

150682560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3781114-C-G

http://identifiers.org/hco/6/GRCh38#150682923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3781613-A-C

150683511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3782147-T-C

http://identifiers.org/hco/6/GRCh38#150683533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3782169-C-A

150683533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3782169-C-T

150683660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3782292-T-G

150683661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3782293-A-G

150683661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3782293-A-T

150683695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3782324-T-C

150683835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 3782423-A-G

150683997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3782570-G-A

150683997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3782570-G-T

150684001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3782574-G-A

150684001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3782574-G-T

150684127-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3782687-T-G

150684467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3782978-T-G

150684922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3783225-C-T

150685920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3784089-G-A

150686275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3784429-C-T

150686649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3784746-T-G

150686739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3784831-G-T

http://identifiers.org/hco/6/GRCh38#150686813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3784910-C-A

150686813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3784910-C-T

150686821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 3784918-G-A

150686893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 3784979-G-T

150687675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3785738-A-G

150687731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3785794-T-G

http://identifiers.org/hco/6/GRCh38#150687881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3785943-A-C

150688835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3787648-T-C

150689321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3788112-G-A

150689330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3788121-A-G

150689429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3788195-G-T

150689796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3788669-A-G

150689818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3788691-G-A

150689928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3788799-T-C

150689928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3788799-T-G

150689965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3788837-T-C

150690984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3789748-A-G

150691573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3790048-C-T

150691614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3790089-T-G

http://identifiers.org/hco/6/GRCh38#150691653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3790135-C-A

150691988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3790444-C-T

150692630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3791434-G-C

150692750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3791558-A-G

150692804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3791620-A-G

150693043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3792990-A-G

150693596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3793492-T-C

150693684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3793582-C-T

150693819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3793688-A-G

150693970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3793799-G-T

150694958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3794440-G-A

150694995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3794477-T-C

150695163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3794626-A-G

150695368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3794802-T-C

150695394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3794828-A-G

150696112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3795510-G-A

150696310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3795700-C-T

150696444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3795783-C-G

150696464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3795803-T-C

150696603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3795937-A-G

150696642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3795967-T-C

150697439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3797003-G-A

150697458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3797036-G-A

150697717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3797295-C-T

150698569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798023-C-T

150698637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798088-C-G

150698637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798088-C-T

150698672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798124-T-C

150698711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798162-G-A

150698884-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798350-A-T

150699360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798783-C-T

150699426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3798857-G-A

150699908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3799425-T-C

150699993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3799507-T-C

150700231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3799766-C-T

150700413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3799909-C-T

150700511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3799989-A-G

150700920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3800699-G-A

150700990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3800759-T-C

150705088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3801181-G-A

150705135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3801215-A-G

150705178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3801317-C-T

150705222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3801362-T-C

150705430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3801568-A-G

150705464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3801605-C-G

150705505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3801661-A-G

150705668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3801838-T-C

150705852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3801999-G-A

150705852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3801999-G-T

150708542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3802594-G-A

http://identifiers.org/hco/6/GRCh38#150709620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3804640-A-C

150709625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3804645-G-C

150710027-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3804809-T-A

150710081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3804863-A-G

150710459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3805192-A-T

150710462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3805195-G-A

150710490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3805215-C-T

150710491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3805216-G-A

150710491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3805216-G-C

150711538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3806859-C-G

150711761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3807102-T-A

150711778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3807119-T-C

150711952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3807271-C-T

150711953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3807272-A-G

150712102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3807447-G-A

150712118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3807463-G-T

150712330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3807695-C-G

150712711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808127-A-T

150712890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808319-T-A

150712993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808429-C-G

150713002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808438-A-G

150713005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808441-A-G

150713160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808617-T-A

150713160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808617-T-C

150713298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3808747-T-C

150713876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809291-G-A

150713991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3809369-G-A

150716163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3810669-A-G

150716289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3810788-A-G

150716304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3810803-C-T

150716325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3810834-C-T

150716345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3810854-A-G

150716362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3810871-C-T

150717625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3812145-C-T

http://identifiers.org/hco/6/GRCh38#150719610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3812368-A-C

150719658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3812407-T-A

150719658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3812407-T-C

150719660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3812409-G-A

150719660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3812409-G-C

150719920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3812678-G-A

http://identifiers.org/hco/6/GRCh38#150719988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3812745-C-A

150720039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3812796-T-C

150720266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3813077-T-C

150720771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3813482-G-A

150720791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3813502-C-G

150721146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3813862-A-G

150721228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3813940-G-A

150721228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3813940-G-T

150721246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 3813951-A-G

http://identifiers.org/hco/6/GRCh38#150721257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#3813962-C-A

150721394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3814131-A-G

150722093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3814846-A-G

150722122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3814861-A-G

150722941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3815283-T-C

150723174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3815503-G-A

150723903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3816446-G-T

150723968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3816486-C-T

150727975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3817226-C-G

150728025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3817271-C-T

150728287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3818318-A-G

150729368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3818508-C-T

150729606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3818741-A-G

150729664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3818799-C-T

150729806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3819788-C-T

150730132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3820003-T-C

150730182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3820050-G-A

150730182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3820050-G-T

150730218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3820087-G-T

150731122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3821003-C-T

150731368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3821250-T-C

150731416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3821294-A-G

150731497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3821373-C-T

150731555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3821425-A-G

150731752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3821619-A-G

150731758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3821625-C-T

150732990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3822373-C-T

http://identifiers.org/hco/6/GRCh38#150733052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3822422-A-C

150733104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3822473-A-G

150733229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3822594-T-C

150733308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3822683-G-C

150733374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3822749-C-T

150733375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3822750-G-A

http://identifiers.org/hco/6/GRCh38#150734143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3823498-C-A

150734326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3823687-C-T

150734374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3823740-G-A

150734527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3823904-A-T

150734562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3823988-G-A

150734651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3824082-G-A

150734890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3824294-G-A

150734988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3824361-T-A

150735756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3828556-C-T

150735824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3828628-G-A

150735914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3828718-A-G

http://identifiers.org/hco/6/GRCh38#150738283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3828953-C-A

150738718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3829384-G-A

150738796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3829471-G-C

150738797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3829472-T-C

150739198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3829861-A-G

150739365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3830019-A-T

150740028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3831232-G-A

150740288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3831484-C-G

http://identifiers.org/hco/6/GRCh38#150740493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3831663-C-A

150740565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3831743-C-T

150740566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3831744-G-A

150740577-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3831755-A-T

150740620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3831797-G-A

http://identifiers.org/hco/6/GRCh38#150740815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3832004-A-C

150740815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 3832004-A-G

150743608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3832699-A-G

150743659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3832751-A-G

150744459-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3833343-A-T

150744600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3833481-A-G

150744745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 3833627-T-A

http://identifiers.org/hco/6/GRCh38#150745777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3834048-C-A

150746173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3834397-A-G

150746184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3834408-A-G

http://identifiers.org/hco/6/GRCh38#150746257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3834449-A-C

150746315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3834495-T-C

http://identifiers.org/hco/6/GRCh38#150746871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3835253-C-A

http://identifiers.org/hco/6/GRCh38#150746876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3835258-C-A

150746876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3835258-C-G

150746922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3835305-C-G

150747008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3835396-C-T

150747027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3835415-T-C

http://identifiers.org/hco/6/GRCh38#150747137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3835534-C-A

150747295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3835692-T-A

150747399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3835791-C-T

150750225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3837173-G-A

150750302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3837253-T-C

150750397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3837347-G-A

150750506-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3837467-G-C

150751286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3838523-T-C

150751382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3838617-G-C

150753388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3841755-A-G

150753462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3841833-C-T

http://identifiers.org/hco/6/GRCh38#150757402-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3844138-A-C

150762392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3844905-T-G

150762395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3844908-C-T

150762591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3845059-T-C

150762618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3845081-G-T

http://identifiers.org/hco/6/GRCh38#150762696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3845149-C-A

150762722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3845170-G-A

150762820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3845253-G-A

150762925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3845343-T-C

150762983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3845401-C-G

150762983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3845401-C-T

150763577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3846665-C-G

150763806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3846850-A-T

150763829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3846873-T-A

150763936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3846980-T-C

150766038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3850313-C-G

http://identifiers.org/hco/6/GRCh38#150766270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3850539-A-C

150766519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3850789-G-A

150766519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3850789-G-C

150766519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3850789-G-T

150766715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3850967-A-G

150766729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3850993-G-A

150766875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3851162-G-A

150766955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3851288-T-C

150766999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3851342-T-G

150767014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3851391-A-T

150767266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3851841-T-A

150767266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3851841-T-C

150767266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3851841-T-G

150767276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3851851-A-T

150767347-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3851921-A-T

150767460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3852045-A-G

150767594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3852169-C-T

150768274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3852944-C-G

150768540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3853460-A-T

150768541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: intron variant
orthologous variants: 3853461-A-T

150768682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: synonymous variant
orthologous variants: 3853601-G-A

150768718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 3853637-G-A

http://identifiers.org/hco/6/GRCh38#150768806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3853724-C-A

150768831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3853749-G-A

150768831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3853749-G-T

http://identifiers.org/hco/6/GRCh38#150769247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3854179-C-A

150770092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3854379-A-G

150770232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3854527-T-C

150770362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3854637-A-G

150770518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3855580-C-T

150770793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3855841-A-G

150770905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3855945-G-A

150771767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3857095-G-T

150772489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3858028-A-T

150772645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3858116-A-G

150772774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3858239-T-C

150773713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3858903-T-A

150773728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3858918-T-G

http://identifiers.org/hco/6/GRCh38#150773948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3859258-A-C

150773948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3859258-A-T

150773957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3859267-G-A

150773982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3859292-C-G

150774219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3859521-A-G

150774219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3859521-A-T

150774225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3859528-T-C

150774305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3859601-G-A

150774497-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3859798-A-T

150774505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3859806-G-T

150774506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3859807-T-C

150774518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3859819-C-T

150775086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3859998-A-G

150775086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3859998-A-T

150775197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3860093-T-A

150775239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3860166-G-A

150775284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3860212-G-A

150775294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3860222-C-T

150775912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3863258-G-C

150776042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3863397-T-A

150776252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3863617-C-G

150779283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3864366-A-G

http://identifiers.org/hco/6/GRCh38#150779319-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3864405-A-C

150779990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3864461-G-C

150780057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3864532-T-A

150780081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3864556-A-G

150780136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3864606-A-T

150783745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3866822-T-C

150783794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3866871-C-T

150783814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3866891-T-C

150784030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3867096-A-G

150784111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3867162-C-T

150784170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3867222-A-G

150784210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3867285-T-A

150784210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3867285-T-G

150784594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3867672-T-C

http://identifiers.org/hco/6/GRCh38#150785072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3868218-A-C

150785100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3868247-G-A

150785139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3868282-T-C

150785159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3868302-G-T

150785230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3868338-C-T

150785436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3868543-A-G

150785503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3868604-T-C

150785696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3868777-A-T

http://identifiers.org/hco/6/GRCh38#150786351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3869094-C-A

150786351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3869094-C-T

150786352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3869095-T-C

150786352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3869095-T-G

150786374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3869117-G-A

150786374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3869117-G-C

150786549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3869298-T-C

http://identifiers.org/hco/6/GRCh38#150786577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3869327-C-A

150786577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3869327-C-T

150786601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3869352-A-T

150786617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3869371-T-A

150786653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3869445-G-C

150787383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3869812-A-G

150787559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3869979-G-T

http://identifiers.org/hco/6/GRCh38#150787878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3870260-C-A

150787878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3870260-C-T

http://identifiers.org/hco/6/GRCh38#150787910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3870284-C-A

150787910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3870284-C-T

150788012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3870393-A-G

150788243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3870622-G-A

150788409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3870787-G-A

150788428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3870806-G-C

http://identifiers.org/hco/6/GRCh38#150788438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3870818-A-C

http://identifiers.org/hco/6/GRCh38#150788498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3870878-C-A

150788539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3870917-G-C

150788731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3871093-A-G

150788732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3871094-C-T

150788743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3871103-G-A

http://identifiers.org/hco/6/GRCh38#150788828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3871172-C-A

150788864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3871209-C-T

150788873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3871218-G-A

150788913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3871269-G-A

150788999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3871338-C-T

150789016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3871351-T-C

150789134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3871461-A-G

150789267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3871588-A-G

150789287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3871604-T-C

150789466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3871805-T-C

150789598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3872234-T-C

150789598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3872234-T-G

150789666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3872299-T-A

150790563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3873199-T-G

150794730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3877781-G-A

150794814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3877866-G-A

150794822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3877874-G-A

150795774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3880126-T-C

150795774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3880126-T-G

150795787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3880139-T-A

150795815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3880166-G-A

150795815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3880166-G-T

150798328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3881245-G-A

http://identifiers.org/hco/6/GRCh38#150798382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3881299-C-A

150799071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3881713-G-T

150799242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3881865-C-T

150799343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3881949-A-G

150799434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3882040-G-C

150799584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3882189-C-G

150799584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3882189-C-T

150799585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3882190-A-G

150799735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3882348-G-A

150799773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3882386-T-C

150799837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3882452-G-A

150800052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3882784-C-T

150800237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883119-C-G

150800505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883327-C-T

http://identifiers.org/hco/6/GRCh38#150800583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3883404-A-C

http://identifiers.org/hco/6/GRCh38#150800600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3883442-A-C

150800621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883495-T-G

http://identifiers.org/hco/6/GRCh38#150800625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3883499-C-A

150800625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883499-C-T

http://identifiers.org/hco/6/GRCh38#150800641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3883515-C-A

150800641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883515-C-T

150800645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883519-T-A

150800691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883568-T-C

150800693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883570-G-T

150800715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 3883593-G-A

150800854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 3883732-T-C

150800863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 3883741-T-C

150800869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 3883747-T-C

150800911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883790-G-A

150800911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883790-G-C

150800914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883793-T-G

150800936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883817-G-A

150800936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883817-G-T

http://identifiers.org/hco/6/GRCh38#150800986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3883878-C-A

150800986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883878-C-G

150800986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883878-C-T

150801016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883908-G-T

150801021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3883913-T-A

150801117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3884010-C-G

150801117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3884010-C-T

150801732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3884502-G-A

150801732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3884502-G-T

150801847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3884602-G-A

150801856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3884611-C-T

150802120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3884998-T-C

http://identifiers.org/hco/6/GRCh38#150802237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3885089-A-C

150802237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3885089-A-G

150802379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3885235-G-A

150802612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3885654-T-A

150803875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3887532-G-C

150803890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3887547-T-G

150803899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3887556-C-T

150804100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3887668-T-G

150804544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3887791-T-C

http://identifiers.org/hco/6/GRCh38#150804592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3887832-C-A

150804592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3887832-C-G

150804592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3887832-C-T

150804651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 3887891-T-C

150804651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 3887891-T-G

150804666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 3887906-T-A

150804729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 3887969-G-A

http://identifiers.org/hco/6/GRCh38#150804732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3887972-C-A

150804751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3887991-C-T

150804780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3888015-G-A

150804780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3888015-G-T

150804804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3888045-A-G

150804804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3888045-A-T

150804826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3888067-G-A

150804826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3888067-G-T

150804896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3888138-T-A

150805319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3888253-T-C

150805330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3888264-G-A

150805394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3888327-G-A

150805480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3888404-C-G

150806053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3888948-G-A

150806214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3889083-T-C

150806214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3889083-T-G

150806234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3889100-T-G

150806247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3889113-T-A

150806247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3889113-T-G

150806254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3889120-G-A

150806254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3889120-G-C

150806254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3889120-G-T

150806321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3889186-A-G

150807354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3889219-C-T

150807367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3889232-C-T

150808983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3890044-A-T

150809091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3890152-A-G

150809091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3890152-A-T

150809253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 3890317-G-A

150809314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3890377-G-A

150809619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3890606-G-T

150812003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3891489-A-G

150812066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3891539-G-C

150812364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3891845-G-A

150812552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3892067-G-C

150812602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3892106-A-G

150812691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3892180-G-A

150812691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3892180-G-T

150812700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3892195-C-G

http://identifiers.org/hco/6/GRCh38#150812875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3892358-A-C

150812875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3892358-A-T

150813481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 3892603-A-T

150813513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 3892639-G-T

150813661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 3892727-G-C

150814302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 3893379-C-G

150814942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3893735-A-G

150814963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3893756-A-G

150815029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3893786-C-T

150815224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 3893991-A-G

150815332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 3894095-C-G

150815692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3894454-C-T

150815707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3894469-C-T

150815724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3894486-C-T

150815801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3894553-G-T

150818034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 3895764-G-T

150818121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 3895851-A-G

150818121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 3895851-A-T

150818150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3895864-A-G

150818338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3897188-T-C

150818611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3897428-T-C

150818624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3897441-T-C

150818624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3897441-T-G

http://identifiers.org/hco/6/GRCh38#150819654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3897495-C-A

150819654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3897495-C-G

150819765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 3897594-A-G

150819843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3897663-G-A

150819843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3897663-G-T

150819861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3897681-G-A

150819861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3897681-G-T

http://identifiers.org/hco/6/GRCh38#150819872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3897691-C-A

150819872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3897691-C-G

150819872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3897691-C-T

150819885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3897692-G-T

150820807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3899082-A-G

150820923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3899170-A-G

150821206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3899678-C-G

150821206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3899678-C-T

http://identifiers.org/hco/6/GRCh38#150821240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3899712-C-A

150821240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 3899712-C-G

150821240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 3899712-C-T

150821249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3899721-T-C

150821252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3899724-T-C

http://identifiers.org/hco/6/GRCh38#150821266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3899737-C-A

150821303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3899770-A-T

150821364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3899838-T-G

150821377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3899851-G-T

150822565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3901350-A-G

150822634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3901421-G-C

150823114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3901800-A-G

150823192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3901869-G-T

150823242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3901914-A-G

150823372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3902037-G-A

150823372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3902037-G-C

150823372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3902037-G-T

http://identifiers.org/hco/6/GRCh38#150823597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3902252-C-A

150823597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3902252-C-T

150823625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3902281-A-G

150823684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 3902341-C-G

150823695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3902352-C-T

150823818-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3902497-T-G

150823886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3902563-C-T

150823919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3902599-T-A

150823966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3902646-A-T

150824016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3902689-A-G

150824104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3902761-C-T

150824203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3903029-T-C

150824325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3903413-G-A

150824456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3903563-G-A

150824992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3904081-G-A

150825241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3904331-G-A

150828682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3905072-A-G

150828703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3905093-T-C

150828856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3905231-A-G

http://identifiers.org/hco/6/GRCh38#150828915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3905285-A-C

150829217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3905565-C-T

150829660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3905826-T-C

150829694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3905864-G-A

150829931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3906095-T-C

150829931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3906095-T-G

150830611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 3906575-G-A

150830611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 3906575-G-T

150830653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 3906611-T-C

150830779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 3906761-A-G

150831187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 3907190-C-T

150831228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3907231-C-G

150831228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3907231-C-T

150831258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3907261-A-G

150831307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 3907310-T-C

150831307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3907310-T-G

150831360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3907363-C-T

150831368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 3907371-C-T

150831568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3907571-C-G

150831789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3907792-T-C

150832072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3908075-T-G

150832126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 3908129-G-A

150832126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 3908129-G-T

150832292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3908289-T-C

http://identifiers.org/hco/6/GRCh38#150832302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3908299-C-A

150832302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3908299-C-T

150832409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3908398-C-G

150834412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3909516-T-C

http://identifiers.org/hco/6/GRCh38#150834707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3909816-A-C

150835191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3910301-T-C

150835193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3910303-T-A

150835265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3910361-G-C

150835284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3910381-G-T

150835812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 3910849-G-T

150837413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3911606-A-G

150837413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3911606-A-T

150837639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3911807-C-T

150838131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3912259-T-C

150838195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3912317-G-C

150838632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3912620-C-T

150838814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3912798-C-G

http://identifiers.org/hco/6/GRCh38#150838852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3912834-A-C

150839565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3913172-C-T

150839666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3913251-G-A

http://identifiers.org/hco/6/GRCh38#150839685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3913266-C-A

150839695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3913276-T-C

150839711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3913292-G-A

150839731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3913303-A-G

150839757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 3913327-G-A

150839855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 3913423-C-T

150839935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3913503-C-G

150839935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3913503-C-T

150840128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 3913699-T-A

150840139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3913710-C-T

150840255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3913829-G-A

150840255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3913829-G-C

150840501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3914075-T-G

150840602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3914176-T-A

150840602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 3914176-T-C

150840602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3914176-T-G

150840611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 3914185-G-A

150840611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3914185-G-T

150840633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 3914207-A-G

http://identifiers.org/hco/6/GRCh38#150840907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3914458-A-C

150841100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3914634-G-A

150841100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3914634-G-T

150841176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 3914639-G-A

150841176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 3914639-G-T

150841196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 3914659-A-T

150841297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 3914748-T-C

150841436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 3914885-T-C

150841524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 3914981-A-G

150842024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3915476-G-A

150842025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 3915477-C-T

150842091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3 prime UTR variant
orthologous variants: 3915543-G-T

150843116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3 prime UTR variant
orthologous variants: 3916752-G-C

150843136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3 prime UTR variant
orthologous variants: 3916774-A-G

150843168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3 prime UTR variant
orthologous variants: 3916806-C-T

http://identifiers.org/hco/6/GRCh38#150843187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#3916828-C-A

150843251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3 prime UTR variant
orthologous variants: 3916888-T-C

150843315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3 prime UTR variant
orthologous variants: 3916942-C-T

150843400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20884
most severe consequence: 3 prime UTR variant
orthologous variants: 3917028-A-G