64987085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76884413-G-A

64987085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76884413-G-T

64987175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76884503-T-C

64987198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76884526-G-A

64987198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76884526-G-C

64987198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76884526-G-T

64987251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76884574-G-A

64987251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76884574-G-C

64987251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76884574-G-T

64987276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76884599-G-T

64987323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76884651-G-A

64987404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76884731-G-A

64987404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76884731-G-T

64987454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76884781-G-A

64987478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 76884805-C-T

http://identifiers.org/hco/14/GRCh38#64987553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76884885-A-C

64987553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76884885-A-T

64987576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76884906-C-G

64987576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76884906-C-T

64987604-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76884917-T-A

64987604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76884917-T-C

http://identifiers.org/hco/14/GRCh38#64987688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76884985-C-A

64987688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76884985-C-T

64987739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76885038-G-C

64987739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76885038-G-T

64988864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76887291-T-C

64988900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76887326-A-G

64989885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76888111-G-A

64989885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76888111-G-C

64989887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76888113-G-C

64989904-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76888130-A-T

64990166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76888438-C-T

64990181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76888487-A-T

64990215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76888653-C-G

64990234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76888671-C-T

http://identifiers.org/hco/14/GRCh38#64990302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76888724-C-A

64990302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76888724-C-G

64990790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76889287-G-A

64999786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76903647-A-G

64999818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76903678-A-G

64999960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76903810-G-A

65000006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76903854-C-T

http://identifiers.org/hco/14/GRCh38#65001998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76904397-C-A

65001998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904397-C-T

65002018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904417-G-T

65003222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904928-A-G

65003222-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904928-A-T

65003241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76904945-T-G

65003307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76905015-C-G

65003331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76905035-G-T

65004127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76909141-T-A

65004127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76909141-T-C

65004211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76909224-A-G

65004227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76909238-C-T

65004244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 76909255-A-G

http://identifiers.org/hco/14/GRCh38#65004278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76909289-C-A

65004278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76909289-C-T

65004326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76909337-T-C

65004336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76909347-A-G

65004337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76909348-G-A

65004337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76909348-G-T

http://identifiers.org/hco/14/GRCh38#65004373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76909366-C-A

65006094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76910196-C-G

http://identifiers.org/hco/14/GRCh38#65006117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76910216-C-A

65006117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76910216-C-T

65006216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 76910272-G-T

65006266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 76910320-T-C

65006346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76910401-A-T

65006413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76910467-A-G

65006494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76910535-C-T

65006635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76910657-G-A

65006716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76910726-C-T

65007262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76912067-C-G

65007607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76912406-G-A

65007805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76913695-C-T

65007950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76913879-G-A

65008259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76914000-T-A

65008428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76914148-G-A

http://identifiers.org/hco/14/GRCh38#65008822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76914330-C-A

65008822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76914330-C-G

65008981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76914493-G-A

65008981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76914493-G-T

http://identifiers.org/hco/14/GRCh38#65009029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76914517-C-A

65009247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76914669-T-G

65010109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76918458-C-G

65010109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76918458-C-T

65010139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76918488-G-A

65010268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76918581-G-A

65010268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76918581-G-C

65011597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76919475-T-C

65011811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76919690-G-T

65011855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76919735-T-G

65012021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76919900-T-C

65012050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76919914-G-A

65012050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76919914-G-T

65012118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76919977-T-C

65012193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76920052-G-A

65012193-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76920052-G-C

65012193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76920052-G-T

65012248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76920107-G-A

65012248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76920107-G-T

65012284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76920118-T-C

65012284-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76920118-T-G

65012292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76920125-G-A

65012375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76920208-A-G

65012517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76920337-G-C

65012517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76920337-G-T

65014863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76921425-T-C

65015475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76921651-A-G

65015505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76921681-G-T

65015506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76921682-A-T

65015512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76921692-G-A

65015512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76921692-G-T

65015554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76921739-A-G

65015584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76921768-A-G

65015750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76921932-C-T

65015757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76921939-T-C

65015779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76921960-G-A

65015779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76921960-G-C

65015779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76921960-G-T

http://identifiers.org/hco/14/GRCh38#65015854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76922036-C-A

65016211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76922718-A-G

65016416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76922927-T-C

65016452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76922959-G-A

65016452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76922959-G-T

65016559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76923058-G-A

http://identifiers.org/hco/14/GRCh38#65016589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76923087-C-A

65016589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76923087-C-T

http://identifiers.org/hco/14/GRCh38#65016915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76923408-A-C

65017431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76923589-T-A

65017450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76923602-G-C

65020058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76926146-T-G

65020080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76926165-C-T

65021046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76926369-A-T

65021086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76926409-G-A

65022101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76927224-A-G

65022152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76927274-G-A

65022192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76927321-G-A

http://identifiers.org/hco/14/GRCh38#65022203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76927330-C-A

65022203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76927330-C-G

65022682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76927927-A-T

65023562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76928681-G-A

65023666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76928770-T-A

65023682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76928791-T-C

http://identifiers.org/hco/14/GRCh38#65023836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76928935-C-A

65023836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76928935-C-T

65023872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76928972-G-A

http://identifiers.org/hco/14/GRCh38#65024092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76929189-A-C

65024217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76929291-A-G

65024229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76929303-A-G

65024933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76930573-G-T

65025038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76930702-C-T

65025086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76930750-C-T

65025115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76930777-A-G

65025296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76930952-G-C

65026192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76932910-G-T

65026224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76932940-A-G

65026929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76934022-C-T

65027282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76934343-A-T

65027305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76934363-A-T

65027325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76934383-G-A

65027325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76934383-G-T

65027453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 76934506-T-C

http://identifiers.org/hco/14/GRCh38#65027543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76934596-A-C

65027543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76934596-A-G

65028952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76937238-T-C

65029067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76937343-T-C

65029505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76937799-T-C

65029692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76938086-C-T

65029715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76938111-G-A

65029715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76938111-G-C

65030139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76942683-T-C

65030207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76942749-G-A

65030404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76942968-C-G

65031507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76943379-G-A

65031552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76943419-G-A

65032092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76943664-C-T

65032289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76943813-A-G

65032332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76943856-A-T

65032337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76943861-G-A

65032337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76943861-G-T

65032370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76943893-T-A

65032429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76943945-T-C

65032491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76944003-G-A

65032491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76944003-G-C

65032501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 76944007-G-T

65032504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 76944010-G-T

http://identifiers.org/hco/14/GRCh38#65032616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76944107-A-C

65032616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76944107-A-G

65032616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76944107-A-T

65032725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76944216-T-C

http://identifiers.org/hco/14/GRCh38#65032783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76944256-C-A

65032783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76944256-C-T

65032847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76944321-T-G

65040416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953231-G-A

65040640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953573-A-G

http://identifiers.org/hco/14/GRCh38#65040695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76953628-C-A

65040695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953628-C-T

65040701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953634-G-A

65040701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953634-G-T

http://identifiers.org/hco/14/GRCh38#65040715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76953648-C-A

65040715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953648-C-T

65040736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953671-T-A

65040853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76953782-C-G

http://identifiers.org/hco/14/GRCh38#65040940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76953868-C-A

65040940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953868-C-G

65040940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953868-C-T

http://identifiers.org/hco/14/GRCh38#65040980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76953902-C-A

65040980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953902-C-T

65040981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953903-A-G

65040990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953912-G-A

http://identifiers.org/hco/14/GRCh38#65041041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76954008-C-A

65041041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76954008-C-G

65041041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76954008-C-T

65041083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76954053-C-G

65041090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76954060-G-A

65041090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76954060-G-T

65041154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76954123-A-G

65041318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76954281-G-C

65041435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76954386-C-T

65041526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76954430-C-T

65041557-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76954458-C-G

65041711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76954606-A-G

65041740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76954637-T-A

65042800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76955724-C-T

65042815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76955731-C-T

65043101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76955995-G-A

65043161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956037-G-A

65043302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956155-T-C

65043321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956174-C-T

65043381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956224-A-G

65044115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956844-T-C

65044186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956907-C-T

65044197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956918-A-G

65044279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956955-T-C

65044281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956957-C-T

65044302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956976-T-C

65044361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76957035-C-T

65044464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957138-A-G

65044471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957145-G-T

65044592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957220-G-A

65044592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957220-G-T

http://identifiers.org/hco/14/GRCh38#65044599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76957227-C-A

65044599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957227-C-T

65044730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76957311-T-G

65044740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76957321-G-A

http://identifiers.org/hco/14/GRCh38#65044776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76957363-C-A

http://identifiers.org/hco/14/GRCh38#65044781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76957368-C-A

65044781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957368-C-G

65044781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957368-C-T

65044782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957369-C-G

65044802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957402-T-C

65044858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957462-G-A

65045028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957964-C-T

65045053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957989-C-G

65045059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957995-C-T

65045091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76958018-A-T

65045142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76958069-T-G

65045198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76958099-A-T

65052622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76960958-T-G

65052657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76960993-G-T

65052693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961016-T-A

65052703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961026-A-T

65052838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961142-T-C

http://identifiers.org/hco/14/GRCh38#65052906-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76961196-A-C

65052908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961198-C-T

65052968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961214-T-C

65053013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961259-G-C

65053013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961259-G-T

http://identifiers.org/hco/14/GRCh38#65053053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76961297-C-A

65053107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961337-G-A

65053107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961337-G-T

http://identifiers.org/hco/14/GRCh38#65053110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76961340-C-A

65053110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961340-C-T

65053126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961356-G-T

65053239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 76961395-T-C

http://identifiers.org/hco/14/GRCh38#65053263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76961419-C-A

65053263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76961419-C-G

65053263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76961419-C-T

65053323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76961479-G-A

65053323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76961479-G-C

65053323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76961479-G-T

http://identifiers.org/hco/14/GRCh38#65053423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76961550-C-A

65053423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961550-C-T

http://identifiers.org/hco/14/GRCh38#65053428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76961555-C-A

65053428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961555-C-G

65053428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961555-C-T

65053483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961617-T-C

65053528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961666-T-C

65053568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76961721-G-A

http://identifiers.org/hco/14/GRCh38#65054442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76963070-C-A

65054442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963070-C-G

65054512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963141-G-T

65054611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76963224-C-T

65054660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76963273-G-A

65054660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 76963273-G-T

http://identifiers.org/hco/14/GRCh38#65054723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76963335-C-A

65054723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963335-C-G

65054778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963405-T-A

65054778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963405-T-C

http://identifiers.org/hco/14/GRCh38#65054814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76963444-C-A

65054814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963444-C-T

65054834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963463-T-G

65054835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963464-T-A

65054836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963465-A-G

65054845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963474-G-A

65055051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963644-C-T

65055206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76963776-C-T

65061143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76966817-C-T

65061152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76966824-T-A

65061152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76966824-T-C

65061152-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76966824-T-G

65061484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76967142-C-T

65061583-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76967248-T-A

65061583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76967248-T-C

http://identifiers.org/hco/14/GRCh38#65061591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76967256-C-A

65061599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76967264-C-T

65061604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76967269-G-T

http://identifiers.org/hco/14/GRCh38#65061776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76967427-C-A

65061786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76967437-G-A

http://identifiers.org/hco/14/GRCh38#65061830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76967479-C-A

65061879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76967521-T-C

65061995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76967623-A-G

65062143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76967760-A-G

65062287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76967873-G-A

65062287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76967873-G-C

65062480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76968003-T-C

http://identifiers.org/hco/14/GRCh38#65062550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76968084-C-A

65062550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76968084-C-G

65062550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3785
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76968084-C-T