62953191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9569227-T-C

62953424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9569044-C-T

62953605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9568868-C-T

62953762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9568719-C-T

62953847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9568638-T-C

http://identifiers.org/hco/3/GRCh38#62953931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9568573-C-A

62953931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9568573-C-G

62954001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9568501-T-C

62955114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9568008-T-C

62955118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9568004-G-A

62955118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9568004-G-C

http://identifiers.org/hco/3/GRCh38#62955147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9567977-C-A

62955189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9567929-A-T

62955319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9567802-G-C

62955427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9566844-T-C

62955550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9566731-C-T

62955594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9566697-A-G

62955628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9566663-G-T

62957315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9566129-A-G

62957499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565962-A-T

62957564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565899-T-G

62957632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565846-A-G

62957632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565846-A-T

62957707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565790-T-C

62957707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565790-T-G

62957721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565776-G-T

http://identifiers.org/hco/3/GRCh38#62957764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9565737-C-A

62957872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565636-G-A

62957921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565589-A-G

62957949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565567-C-T

62958364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565179-G-A

62958366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565177-G-A

62958443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565106-A-G

62958506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565054-T-C

62958532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9565028-C-T

http://identifiers.org/hco/3/GRCh38#62958601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9564961-C-A

62958936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9564756-C-T

62958997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9564695-G-T

62959022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9564669-G-C

62959080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9564606-G-A

62962723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9553409-A-G

62962995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9553672-C-T

62963063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9553731-G-A

62965057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9555906-G-T

62965122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9555965-T-C

62965122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9555965-T-G

62965285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556071-G-T

62965319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556114-A-T

62965323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556117-G-A

62965323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556117-G-C

62965355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556149-G-T

62965491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9556287-T-C

62965797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556469-G-A

62965819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556491-G-A

62965923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556593-T-C

62966040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556702-C-G

62968038-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556933-A-T

62968043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9556938-A-G

62968213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9557117-T-C

62968371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9557259-A-T

62968475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9557351-C-T

62968476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9557352-G-A

62972116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551648-C-T

62972303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551524-A-G

62972454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551369-G-C

62972490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551331-T-C

62972607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551233-G-A

62972608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551232-A-T

62972742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9551118-A-G

62972814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9550981-C-G

62972814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9550981-C-T

62973132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9550662-T-G

62973229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9550564-T-G

62973441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9550395-T-C

62973473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9550365-G-T

62975008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9546297-T-C

62975008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9546297-T-G

62975188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9546133-G-T

http://identifiers.org/hco/3/GRCh38#62975498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9545892-C-A

62975545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9545851-T-A

62975545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9545851-T-C

http://identifiers.org/hco/3/GRCh38#62975682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9545715-A-C

62975977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9544762-C-T

62976100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9544652-A-G

62976186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9544568-T-C

62976186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9544568-T-G

62976227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9544521-T-A

62976279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9544470-G-C

62976279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9544470-G-T

62976293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9544456-C-T

62976350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9544400-T-G

62976741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543992-A-G

62976854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543876-C-T

62976892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543838-A-T

62976901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543829-C-G

62976901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543829-C-T

62976959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543771-C-G

62976994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543743-C-T

62977085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543613-T-C

62977163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543540-G-T

62977304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543411-A-G

62977320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543394-A-T

62977327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543385-C-T

62977349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543356-A-T

62977361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543344-A-G

62977361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9543344-A-T

62978991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9542825-G-A

62978991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9542825-G-C

62978991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9542825-G-T

http://identifiers.org/hco/3/GRCh38#62978998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9542821-C-A

62978998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9542821-C-T

62979028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9542791-A-G

http://identifiers.org/hco/3/GRCh38#62979036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9542783-C-A

62979036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9542783-C-T

62979126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9542696-T-C

62979213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9542607-T-C

62980580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9540269-C-G

62980583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9540266-T-C

62980706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9540144-C-G

62980728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9540122-A-T

62980815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9540049-G-C

http://identifiers.org/hco/3/GRCh38#62980840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9540026-A-C

62981001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539878-G-A

62981107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539778-G-A

62981255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539615-C-T

http://identifiers.org/hco/3/GRCh38#62984308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9539564-C-A

62984448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539417-T-C

http://identifiers.org/hco/3/GRCh38#62984449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9539416-C-A

62984449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539416-C-T

62984494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539377-G-C

62984505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539366-G-A

http://identifiers.org/hco/3/GRCh38#62984523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9539350-C-A

http://identifiers.org/hco/3/GRCh38#62984661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9539222-C-A

62984699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539184-A-G

62984819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9539091-G-A

62984939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538984-T-C

62985080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9538905-T-C

62985732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538468-G-C

62985741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538459-T-C

62985862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538346-A-G

62985868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538340-T-A

62985938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538293-C-T

62985971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538261-C-G

62986104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9538138-A-G

62986550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9537721-C-G

62986566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9537705-T-G

62988542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9535741-A-G

62988614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9535650-C-T

62988686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9535579-A-G

62988711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9535554-T-A

62988819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9535447-G-A

62988846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9535420-T-C

http://identifiers.org/hco/3/GRCh38#62988903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9535363-A-C

62988960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9535306-G-T

62989145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9535109-G-A

62989145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9535109-G-C

62989194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9535060-T-C

62989298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9534953-A-G

62989328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9534923-G-A

62989524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9534741-G-C

62990505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9531295-C-T

62990509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9531291-G-A

62990530-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9531273-C-G

62990589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9531211-G-A

62990589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9531211-G-T

62990743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9531063-T-C

62990949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9530868-G-C

62991032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9530780-C-T

62991035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9530777-C-T

62991089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9530724-A-G

62991151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9530651-G-A

62991167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9530635-G-C

62991278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9530524-G-T

62991411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9530389-G-A

http://identifiers.org/hco/3/GRCh38#62991415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9530385-C-A

62991415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9530385-C-T

62991430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9530368-G-A

http://identifiers.org/hco/3/GRCh38#62995805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9526382-C-A

62995832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9526354-A-G

62995860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9526326-C-T

62995867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9526319-C-G

62995892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9526294-T-A

62996040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9526142-T-A

62996110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9526099-T-C

62996116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9526093-C-T

62996186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9526030-A-T

http://identifiers.org/hco/3/GRCh38#62996200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9526016-C-A

62996200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9526016-C-G

62996200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9526016-C-T

62996910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9524986-T-A

62996939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9524973-T-C

62997053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9524890-T-C

62997111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9522105-C-T

62997187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9522032-G-A

62997204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9522011-G-T

62997260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9521962-A-G

62997266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9521956-T-C

62997347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9521877-T-G

62997441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9521796-T-C

62997444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9521793-A-G

http://identifiers.org/hco/3/GRCh38#62997551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9521687-C-A

62997621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9521616-G-C

62997745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9521515-C-T

62997964-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9519488-T-A

62997964-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9519488-T-G

62997998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9519456-A-G

62998012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9519442-A-G

62998031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9519424-C-T

62998384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9519077-G-A

62998584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9518859-C-T

62998662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9518738-C-T

62998745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9518660-C-T

62998836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9518581-G-A

62998950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9518478-A-T

62999071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9518367-A-T

62999150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9518264-T-C

62999156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9518112-C-G

62999156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9518112-C-T

62999196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9518073-A-G

62999204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9518065-C-T

62999209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9518061-A-G

62999321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9517950-G-A

62999351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9517920-C-T

http://identifiers.org/hco/3/GRCh38#62999468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9517822-A-C

http://identifiers.org/hco/3/GRCh38#62999619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9515779-A-C

62999619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9515779-A-G

62999654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9515730-A-G

62999745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9515646-T-C

62999746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9515645-C-G

62999776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9515615-C-G

63000072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9515351-T-A

63000315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9515109-C-T

http://identifiers.org/hco/3/GRCh38#63000429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9514993-C-A

63000498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514925-G-T

63000513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514910-T-C

63000598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514834-G-T

63000634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514799-G-A

63000634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514799-G-T

63000708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514741-T-C

63000709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514740-T-C

63000709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514740-T-G

63000732-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514731-T-G

63000746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514717-T-C

http://identifiers.org/hco/3/GRCh38#63000751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9514712-A-C

http://identifiers.org/hco/3/GRCh38#63000761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9514702-C-A

63000902-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514642-C-G

63000902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514642-C-T

63000955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514592-T-C

http://identifiers.org/hco/3/GRCh38#63000970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9514577-C-A

63001047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514499-C-T

http://identifiers.org/hco/3/GRCh38#63001083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9514463-A-C

63001219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514328-G-T

63001301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514253-G-A

63001318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9514238-C-T

63001732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9513326-T-C

http://identifiers.org/hco/3/GRCh38#63001789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9513269-C-A

63001835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9513204-T-G

63001857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9513178-G-A

63002069-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9513010-C-G

63006115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9501651-C-T

63006139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9501627-G-A

63006265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9501502-G-A

63006265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9501502-G-T

63006274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9501493-T-C

63006293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9501473-C-T

63006579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9501213-G-A

63006848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9500949-G-A

63006872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9500925-A-G

63008880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9497342-A-G

63008944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9497271-A-G

63008994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9497221-C-G

63019742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9496738-C-T

63019755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9496728-T-C

63019850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9496655-C-T

63019973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9496532-A-G

63020713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9496251-A-G

63020728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9496236-T-C

63021004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9495968-A-G

63021042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9495930-T-C

http://identifiers.org/hco/3/GRCh38#63021138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9495834-C-A

http://identifiers.org/hco/3/GRCh38#63021139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9495833-C-A

63021457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9495784-T-C

63021683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9494729-A-G

63021931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9494529-T-C

63022141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9494341-C-T

63022185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9494295-C-T

63022269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9494212-A-G

http://identifiers.org/hco/3/GRCh38#63022561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9493926-A-C

63022808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9493691-C-T

63022858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9493647-C-T

63023000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9493520-C-G

63023164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9493358-A-G

http://identifiers.org/hco/3/GRCh38#63023201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9493324-C-A

63023227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9493299-T-A

63023980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9492925-T-G

63024058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9492849-T-C

63024206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9492751-C-G

63024206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9492751-C-T

63024761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9492346-G-C

63025061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9492194-T-C

http://identifiers.org/hco/3/GRCh38#63025081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9492174-C-A

63025563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

http://identifiers.org/hco/3/GRCh38#63029279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9490735-C-A

63029279-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9490735-C-G

63029307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9490716-C-T

http://identifiers.org/hco/3/GRCh38#63029382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9490648-A-C

63029454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9490577-G-C

63029454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9490577-G-T

63029458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9490573-G-A

63029458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9490573-G-C

63029588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9490472-C-T

63030044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9490357-C-T

63033199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9487543-C-T

63033486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9487261-A-G

63033495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9487251-T-A

63033495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9487251-T-C

63033592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9487162-A-G

63034438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9486360-C-G

63034471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9486325-C-T

63034846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9483275-G-C

63034850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9483271-G-C

63035064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9483055-G-C

63037620-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9471567-T-G

63037626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9471561-T-C

63038983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9471185-T-C

63039965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9470835-G-A

63040004-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9470798-C-G

63040086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9470733-C-T

63040103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9470716-A-G

http://identifiers.org/hco/3/GRCh38#63040124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9470696-A-C

63040234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9470588-G-A

63040234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9470588-G-C

63040235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9470587-T-C

63040475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9470420-G-A

http://identifiers.org/hco/3/GRCh38#63040564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9470329-A-C

63040578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9470315-T-C

63042680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9469724-C-G

63042970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9469432-C-G

63043147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9469256-C-G

63043176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9469227-T-C

63043259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9468878-C-G

63043278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9468859-A-G

63043315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9468818-T-C

http://identifiers.org/hco/3/GRCh38#63043330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9468803-C-A

63043368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9468765-C-G

63043392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9468740-G-C

63043694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9468527-G-A

63043729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9468509-A-G

63043762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9468476-C-T

63044128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9468118-A-G

63044186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9468054-A-T

63044197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9468043-G-A

63044197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9468043-G-T

http://identifiers.org/hco/3/GRCh38#63044254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9467985-C-A

63044352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9467891-G-A

63045238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9465455-C-T

63045280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9465413-T-C

63045307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9465381-C-T

63045329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9465360-C-T

63045425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9465263-T-A

63045425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9465263-T-G

63045496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9465190-G-A

63045607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9465079-A-G

63045682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9464856-C-G

63045701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9464837-A-G

63046032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9464354-A-G

63046104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9464326-A-G

63046197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9464244-G-T

63046353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9464114-G-T

63046630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9463879-G-C

63046713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9463827-C-T

http://identifiers.org/hco/3/GRCh38#63046845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9463725-A-C

63047183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9463447-A-G

63047318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9463327-C-T

63047330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9463315-G-A

63047330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9463315-G-T

63047413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9463242-C-T

63047449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9463186-G-A

63047507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9463147-T-A

63047747-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9462630-T-G

63048020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9462355-G-T

63048695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460595-C-G

63048695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460595-C-T

63048705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460586-T-C

63048764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460527-C-T

63048837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460460-T-C

63048862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460438-G-A

63048881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460428-G-T

63049031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460279-G-A

63049035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460275-T-C

63049036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460274-A-G

http://identifiers.org/hco/3/GRCh38#63049086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9460220-C-A

63049086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460220-C-G

63049086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460220-C-T

63049140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460168-T-C

63049204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460141-A-G

http://identifiers.org/hco/3/GRCh38#63049306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9460069-C-A

63049306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460069-C-T

63049343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9460036-C-G

63049483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9459907-G-T

63049506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9459883-G-A

63049554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9459836-G-C

63049554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9459836-G-T

63049575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9459815-C-T

63049582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9459808-C-G

http://identifiers.org/hco/3/GRCh38#63049885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9458417-C-A

63049996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9458315-C-T

63050053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9458252-C-G

63050079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9458226-C-T

63050581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9457914-C-T

http://identifiers.org/hco/3/GRCh38#63050804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9456679-C-A

63050822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9456661-G-C

63050822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9456661-G-T

63051184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9456345-C-G

http://identifiers.org/hco/3/GRCh38#63051244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9456273-C-A

63051318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9456198-A-G

63051461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9447431-G-A

63051778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9447065-T-C

63051819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9447024-C-T

63051914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9446931-G-A

63052017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9446846-G-T

63052739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9446225-C-G

63052739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9446225-C-T

63052849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9446141-A-G

63052859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9446131-G-T

63053004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9446000-A-G

63053028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9445963-G-A

63053049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9445923-T-G

63053391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9445454-G-T

63053422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9445424-C-T

63053548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9445306-A-T

http://identifiers.org/hco/3/GRCh38#63053567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9445289-A-C

63053567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9445289-A-G

63054503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9444748-C-T

63054514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9444735-G-T

63054649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9444615-C-T

63054745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9444534-A-G

http://identifiers.org/hco/3/GRCh38#63054790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9444491-C-A

63054790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9444491-C-T

63054799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9444482-C-G

http://identifiers.org/hco/3/GRCh38#63054918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9444373-A-C

http://identifiers.org/hco/3/GRCh38#63054923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9444368-C-A

63055196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9443877-T-C

63055598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9443391-T-C

63055634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9443357-A-G

63055686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9443309-A-G

63055862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9443149-A-G

63055893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9443122-A-G

63057383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9440832-C-G

63057460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9440757-C-G

63057556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9440637-C-T

http://identifiers.org/hco/3/GRCh38#63057574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9440617-C-A

63057815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9440398-G-T

63058038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9440165-T-G

http://identifiers.org/hco/3/GRCh38#63058111-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9440090-C-A

63058111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9440090-C-T

63058188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9439850-A-G

63058237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9439801-G-A

63058286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9439753-T-C

63058354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9439682-A-G

63058376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9439660-A-G

63058577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9439384-T-A

63058639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9439329-T-A

63058657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9439312-T-C

63058754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9439213-G-A

http://identifiers.org/hco/3/GRCh38#63058786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9439181-C-A

63059244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9437829-T-C

63059258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9437815-A-G

63059300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9437774-T-C

63059337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9437743-T-C

63059406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9437681-G-T

63059559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9437534-C-T

63059788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9437161-A-T

63059881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9437063-C-T

63060412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9436505-T-C

63060485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9436437-T-G

63060509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9436413-C-T

63060575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9436376-C-T

63060821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9436132-G-T

http://identifiers.org/hco/3/GRCh38#63060931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9436022-C-A

63061073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9435891-T-G

63061096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9435860-C-T

63061097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9435859-G-A

63061163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9435824-A-G

63061288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9435692-G-A

63061323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9435654-C-T

63061428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9435573-C-T

63061548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9435484-A-G

63061711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9435359-C-T

63061717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9435353-T-C

63061886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9435213-C-T

63061896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9435204-A-G

63062583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9433986-A-G

63062630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9433939-T-C

63062681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9433889-C-T

63062817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9433764-C-T

63063000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9433376-G-A

63063118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9433261-C-T

63063135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9433245-G-T

63063475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9432894-T-C

http://identifiers.org/hco/3/GRCh38#63063481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9432888-C-A

63063481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9432888-C-G

63063528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9432842-A-G

63063600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9432803-C-T

63063619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9432786-T-G

63063647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9432757-G-A

63064630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9432107-G-C

63064794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9431949-G-A

63064866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9431872-G-A

63065015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9431737-T-C

63065127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9431590-A-G

63065127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9431590-A-T

63065201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9431524-C-T

63065372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9431358-C-G

63065379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9431352-A-T

http://identifiers.org/hco/3/GRCh38#63065507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9431249-A-C

63066003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9430608-A-T

63066095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9430552-C-G

63066225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9430422-A-G

63066248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9430399-T-A

63066306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9430348-A-G

63066325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9430329-G-C

63066552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9430131-G-T

63066584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9430104-C-T

63066978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9429827-C-G

http://identifiers.org/hco/3/GRCh38#63067165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9429645-C-A

63067165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9429645-C-G

63067165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9429645-C-T

63067259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9429561-T-C

63067413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9429404-C-T

63067414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9429403-G-A

63067481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9429337-A-G

63067485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9429333-T-A

63067497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9429321-G-A

63068902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9427988-T-A

63068959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9427931-C-T

63068966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9427924-G-A

63069357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9427537-G-A

63069454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9427438-C-T

63069649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9426676-C-G

63069811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9426570-G-A

63069817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9426564-G-A

63069969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9426424-G-A

63070389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9426021-G-A

63070546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9425893-C-T

63071993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9422513-G-T

63072037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9422465-G-C

63072132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9422370-T-C

63072620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9421881-G-T

63072665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9421852-T-A

63072949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9421705-T-C

63073040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9421622-C-G

63073044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9421618-A-G

63073104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9421573-A-G

63073104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9421573-A-T

63073212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9421477-A-G

63073328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9421317-G-C

63073515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9421143-G-A

63073846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9420853-G-T

63074148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9420553-T-C

63074395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9420312-G-A

http://identifiers.org/hco/3/GRCh38#63074789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9419976-C-A

63074844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9419921-G-A

63074844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9419921-G-C

63074936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9419833-G-A

63075068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9419600-C-G

63075516-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9418477-G-C

63075668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9418336-A-G

63075668-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9418336-A-T

63075675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9418329-T-C

63075740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9418267-A-T

63076149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9418099-C-T

63076341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9417909-G-A

http://identifiers.org/hco/3/GRCh38#63076439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9416882-A-C

63076448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9416873-G-T

http://identifiers.org/hco/3/GRCh38#63076490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9416828-C-A

63076560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9416768-C-T

63076669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9416684-T-G

63076729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9416630-C-T

63076748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9416614-T-C

63076806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9416563-T-G

63076828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9416548-G-A

63076860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9416518-C-T

63076868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9416510-C-T

63077063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9416118-C-T

63077080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9416101-G-A

63077158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9416023-G-A

63077192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9415979-C-T

63077941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9415062-G-A

63078232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9414795-C-G

63078273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9414755-T-G

63078274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9414754-G-T

63078345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9414696-T-C

63078376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9414663-C-T

63078377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9414662-G-A

63078377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9414662-G-T

63078583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9414447-G-A

63078639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9414394-G-A

63078758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9414275-A-G

63079209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9413318-G-A

63080527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9411661-A-G

63080650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9411539-G-A

63080656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9411533-G-A

63080777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9411400-T-C

63080777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9411400-T-G

63080792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9411387-C-T

63080803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9411376-C-T

63081130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9411115-T-C

63081210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9410941-A-G

63081217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9410934-T-C

63081224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9410927-G-A

63081672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9410511-A-G

63081805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9410361-G-A

63081864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9410298-A-T

63085160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9408254-A-G

63086148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9402900-G-C

63086241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9402803-G-A

http://identifiers.org/hco/3/GRCh38#63086367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9402669-C-A

63086367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9402669-C-G

63086367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9402669-C-T

63086389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9402647-C-G

63086395-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9402640-G-T

63086439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9402480-A-G

63086443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9402476-G-C

63086447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9402472-T-C

63086455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9402464-A-G

63086455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9402464-A-T

63086808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9402116-A-G

63088288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9400053-C-G

63088364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9399978-G-A

63088701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9398906-C-T

63088805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9398799-A-G

63088947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9398671-G-A

63088978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9398639-G-A

63088978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9398639-G-T

http://identifiers.org/hco/3/GRCh38#63089116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9398522-C-A

63089313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9398328-T-A

63089405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9398245-T-A

63089484-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9398188-T-C

63089699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9397984-T-C

63090073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9397692-G-A

63090093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9397677-A-G

63090159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9397628-C-T

63090247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9397556-T-G

63091935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9396782-C-T

63092263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9396468-T-A

63092424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9396308-G-A

63092424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9396308-G-T

63092688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9395913-A-T

63092804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9395800-A-G

63092993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9395266-T-C

63093294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9394995-A-G

63093365-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9394698-T-A

63093401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9394662-C-T

63095345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9394329-T-G

63095406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9394279-C-T

63095621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9394049-T-C

63095621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9394049-T-G

63095859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9393735-C-G

63099048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9393099-T-A

63099095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9393060-G-T

63099101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9393044-G-C

63099127-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9393014-T-A

63099217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392936-G-T

63099250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392905-A-G

63099328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392827-G-A

63099386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392774-G-A

63099386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392774-G-T

63099413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392747-C-T

63099440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392717-C-T

63099447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392710-A-G

63099458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392699-A-G

63099476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392682-G-A

63099582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9392576-T-C

63099589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 9392569-G-A

63099806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9392319-G-A

63101941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9391794-C-T

63101986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9391749-T-C

http://identifiers.org/hco/3/GRCh38#63102081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9391655-C-A

63102081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9391655-C-T

63102268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9391469-A-G

63102396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9391337-A-G

63102430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9391308-A-G

63102435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9391303-C-T

63102505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9391230-A-G

63102505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9391230-A-T

63102528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9391205-C-T

63102651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9391075-A-G

63102733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9390984-A-G

63102872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9390860-A-G

63102888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9390827-T-C

63102900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9390815-C-T

63102902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9390813-A-G

63102925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9390786-G-C

63102925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9390786-G-T

63103218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9389467-T-C

63103219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9389466-G-A

http://identifiers.org/hco/3/GRCh38#63103672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9389023-A-C

63103867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9388867-A-T

63103876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9388858-C-G

63103876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9388858-C-T

63103962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9388778-T-C

63104175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387574-A-G

63104327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387445-C-T

63104354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387418-C-T

63104480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387298-C-T

http://identifiers.org/hco/3/GRCh38#63104533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9387249-C-A

63104533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387249-C-T

http://identifiers.org/hco/3/GRCh38#63104559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9387227-C-A

63104559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387227-C-T

63104582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387204-G-T

63104642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387136-C-T

http://identifiers.org/hco/3/GRCh38#63104664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9387115-A-C

63104700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387083-T-C

63104714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387069-A-T

63104717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387066-G-T

63104745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387022-A-G

63104751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9387016-T-C

63104888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384885-T-C

63104964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384824-A-G

63104964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384824-A-T

63104977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384811-C-T

63104978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384810-G-A

63105177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384640-G-A

63105292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384563-C-G

63105351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384514-C-G

63105396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384471-G-T

63105484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384383-G-A

http://identifiers.org/hco/3/GRCh38#63105492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9384375-C-A

63105733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384199-G-T

63105754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384186-T-C

63105842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384130-T-C

63105848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384124-T-C

http://identifiers.org/hco/3/GRCh38#63105853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9384119-C-A

63105853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384119-C-G

63105859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9384106-G-T

http://identifiers.org/hco/3/GRCh38#63105912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9384055-C-A

63106019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9382851-C-G

63106019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9382851-C-T

63106060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9382817-T-C

http://identifiers.org/hco/3/GRCh38#63106064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9382815-A-C

63106118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9382572-A-G

63106203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9382489-C-T

http://identifiers.org/hco/3/GRCh38#63106259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9382438-C-A

63106423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 9382273-G-A

63106553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382116-T-A

63106553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382116-T-C

63106556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382103-A-G

63106576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382072-G-C

63106673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9382000-C-T

63106692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9381977-C-T

63106693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9381976-A-T

63106728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9381941-C-T

63106759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9381908-C-T

63107117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9381557-C-T

63108137-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9376962-C-G

63108137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9376962-C-T

63108284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9376802-G-T

63108464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9376666-C-G

63108495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9376642-G-T

63108626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9376510-C-T

63109013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9376127-T-A

63109020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9376121-G-A

63109060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9376091-G-A

63109253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9375897-T-C

63109348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9375811-G-A

63109413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9375748-C-G

63109413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9375748-C-T

63109414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9375747-A-G

63109428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9375733-G-C

63113284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9366720-C-T

63113286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9366718-A-G

63113354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9366652-T-C

63113400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9366611-C-G

63113400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9366611-C-T

63113524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9366491-G-T

63113557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9366458-C-T

http://identifiers.org/hco/3/GRCh38#63113616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9366399-C-A

http://identifiers.org/hco/3/GRCh38#63113704-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9366333-A-C

63113780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9366266-A-G

63113781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9366265-T-A

63113813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9366233-G-T

63113873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9366181-G-A

63113953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9366098-G-T

63114012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9366045-A-G

63114130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9365929-G-A

63114130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9365929-G-T

63114411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9365635-A-G

63114844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9365249-G-A

63114947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9365159-G-C

63114947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9365159-G-T

63117595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9361860-G-C

63117606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9361849-G-A

63117606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9361849-G-C

http://identifiers.org/hco/3/GRCh38#63117680-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9361775-A-C

63117865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9361609-G-T

63118084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9361402-G-C

63118356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9361172-A-G

http://identifiers.org/hco/3/GRCh38#63118399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9361131-C-A

63118431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9361100-C-T

63118497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9361018-G-T

63118498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9361017-G-C

63118553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9360781-A-G

http://identifiers.org/hco/3/GRCh38#63118580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9360754-C-A

63118583-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9360751-C-G

63118583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9360751-C-T

http://identifiers.org/hco/3/GRCh38#63118632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9360704-C-A

63118769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 9360247-G-T

63119781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9358216-A-G

63119937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9358075-G-A

63119937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9358075-G-T

63119983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9358042-C-T

63120100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9357947-G-A

http://identifiers.org/hco/3/GRCh38#63120176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9357885-C-A

63120461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9357619-G-T

63122531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9355976-G-T

63122563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9355943-T-A

63122698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9355810-G-A

http://identifiers.org/hco/3/GRCh38#63122875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9355627-A-C

63122875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9355627-A-G

63123107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9355438-A-T

63123129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9355417-T-A

63123229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9355338-A-G

63123229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9355338-A-T

http://identifiers.org/hco/3/GRCh38#63123288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9355287-C-A

63123304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9355271-T-C

63123412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9355020-A-G

63123692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9354765-T-C

http://identifiers.org/hco/3/GRCh38#63123801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9354661-C-A

63123827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9354635-T-C

63123998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 9354484-T-C

http://identifiers.org/hco/3/GRCh38#63124084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9354381-C-A

63124092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9354373-G-C

63124146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9354322-A-G

http://identifiers.org/hco/3/GRCh38#63124176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9354292-C-A

63124176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9354292-C-G

63124176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9354292-C-T

63124193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9354276-G-T

63124346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9354164-G-A

63124346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9354164-G-T

63124464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9354050-T-A

63124468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9354046-C-T

63124510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9354008-T-C

http://identifiers.org/hco/3/GRCh38#63124544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9353978-C-A

63124544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9353978-C-T

63124563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9353959-T-C

63124574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9353949-T-C

63124657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9353866-G-A

63124657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9353866-G-T

http://identifiers.org/hco/3/GRCh38#63124764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9353757-C-A

63124764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9353757-C-T

63124767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9353754-C-T

63124781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9353740-A-G

63124784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9353737-G-A

http://identifiers.org/hco/3/GRCh38#63124790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9353731-C-A

63124790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9353731-C-T

63124891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9353672-C-T

63124998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9353488-T-C

http://identifiers.org/hco/3/GRCh38#63125047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#9353440-C-A

63125047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27720
most severe consequence: non coding transcript exon variant
orthologous variants: 9353440-C-T