101492587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 37233450-G-T

101492963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37233860-G-T

101492975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37233872-A-T

http://identifiers.org/hco/8/GRCh38#101492977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#37233874-C-A

101493362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37234262-T-C

101493572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37234406-G-A

101493572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37234406-G-T

101493693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37234515-G-A

101493960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37234750-C-T

101494025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37234813-G-A

http://identifiers.org/hco/8/GRCh38#101494137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37234924-C-A

101494369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37235077-G-C

101494506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37235212-C-T

101495178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37236321-T-C

101495544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37236913-T-C

101496224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37237492-A-G

101496691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37237847-A-T

101497064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37238243-C-T

101497406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37238582-T-G

101497796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37238991-C-T

101497876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37239073-G-A

101497876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37239073-G-T

101497937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37239137-T-C

101499265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37239914-C-T

101499393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37240550-C-T

101499429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37240582-G-T

http://identifiers.org/hco/8/GRCh38#101499591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37240687-C-A

101499591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37240687-C-G

101500243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37241001-G-A

101500364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37241093-C-G

101500646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37241412-C-G

101500992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37241808-T-C

http://identifiers.org/hco/8/GRCh38#101501030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37241847-C-A

101501030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37241847-C-T

101501373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37242202-C-T

101501432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37242253-T-G

101501446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37242339-G-A

101501514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37242468-A-T

101501725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37242683-G-A

101501942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37242858-A-T

101502234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37243128-C-T

101502252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37243147-T-C

101502256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37243151-A-G

101502270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37243166-A-G

101502586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37243445-G-A

http://identifiers.org/hco/8/GRCh38#101502733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37243562-C-A

101502733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37243562-C-T

101502813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37243650-T-C

101504622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37247251-T-C

101504761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37247322-C-G

101505048-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37247531-T-G

http://identifiers.org/hco/8/GRCh38#101506186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37249062-A-C

101508730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37250192-C-T

101509534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37251976-G-T

101509751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37252160-G-A

101509773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37252180-A-G

101513824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37255163-C-T

101514090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37255466-A-T

http://identifiers.org/hco/8/GRCh38#101514393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37255851-A-C

101515234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37256419-G-T

101516009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37257157-A-G

101516010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37257158-G-A

101516226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37257279-C-T

101516904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37257777-T-C

101518982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37258969-G-T

101519073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37259283-T-A

101519627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37259515-T-C

101519663-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37259551-A-T

101521104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261243-G-A

101521124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261257-C-T

101521158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261295-G-C

101521252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261371-G-A

101521289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261392-G-A

101521313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261412-A-G

101521323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261422-G-T

101521357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261456-C-T

101521391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261489-C-T

101521567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261605-T-G

101521779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37261842-A-T

101521910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37261970-C-G

101521994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37262036-G-A

101522032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 37262065-G-C

101534929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37265946-C-G

101535351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37266259-C-T

101538351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37267115-C-T

101538463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37267197-T-A

http://identifiers.org/hco/8/GRCh38#101538477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37267211-C-A

101538485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37267212-G-C

101539030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37267843-G-A

101539098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37267890-G-C

101539266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37267993-T-C

101539294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37268023-A-G

101539374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37268219-T-C

101539454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37268284-C-G

101539721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37268499-C-G

101539721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37268499-C-T

101539866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37268662-C-T

101540108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37268957-T-C

101540123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37268972-T-C

http://identifiers.org/hco/8/GRCh38#101540169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37269016-A-C

101541597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37269284-C-T

101541929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37269599-C-T

101542012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37269669-C-T

http://identifiers.org/hco/8/GRCh38#101542036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37269693-C-A

101542138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37269803-G-A

101542249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37269898-C-G

101542249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37269898-C-T

101543063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37270655-A-G

101543171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37270762-A-G

101543406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37270999-T-G

101543444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 37271037-C-T

101543499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37271077-A-G

101543566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37271120-G-A

101543566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37271120-G-T

http://identifiers.org/hco/8/GRCh38#101543593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37271137-C-A

http://identifiers.org/hco/8/GRCh38#101543599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37271143-C-A

101543599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37271143-C-G

101543600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 37271144-A-G

101545745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37272487-G-A

101545796-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37272538-T-A

101545806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37272551-A-G

http://identifiers.org/hco/8/GRCh38#101545848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37272593-C-A

101546322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37273008-G-A

101546880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37273157-T-C

http://identifiers.org/hco/8/GRCh38#101547021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37273282-A-C

101547051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37273316-T-C

101551382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37274042-G-C

101551404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37274064-C-G

101551415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37274075-G-A

101551558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37274216-G-A

101551614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37274271-G-A

101551614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37274271-G-C

101552584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37274773-T-C

101552614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37274797-A-G

101552663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37274846-T-C

101552799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37274978-G-A

101552827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37275012-A-G

101552883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37275427-G-A

101552883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37275427-G-C

101552884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37275428-C-T

101552908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37275448-G-A

101552915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37275455-G-A

101552915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37275455-G-C

101552915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37275455-G-T

http://identifiers.org/hco/8/GRCh38#101552917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37275457-C-A

101552917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37275457-C-T

101553231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37275707-G-A

101553237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37275713-C-T

101553284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37275738-A-G

http://identifiers.org/hco/8/GRCh38#101553453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37275879-A-C

101554925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37276156-T-C

101555461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37276630-C-T

101555523-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37276683-A-T

http://identifiers.org/hco/8/GRCh38#101555549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37276710-A-C

101555613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37276774-T-C

101555653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37276813-T-G

http://identifiers.org/hco/8/GRCh38#101555780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37276938-A-C

http://identifiers.org/hco/8/GRCh38#101556514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37277385-A-C

101556514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37277385-A-G

101556817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37277636-C-G

101558521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: synonymous variant
orthologous variants: 37279680-T-C

101558608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: synonymous variant
orthologous variants: 37279767-G-A

101558710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: stop gained
orthologous variants: 37279869-T-A

101558790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: missense variant
orthologous variants: 37279949-G-C

101558819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 37279978-C-T

101558839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37279987-A-G

http://identifiers.org/hco/8/GRCh38#101558874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37280005-C-A

101558875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37280006-T-C

http://identifiers.org/hco/8/GRCh38#101558880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37280011-C-A

101558910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37280035-G-C

101558925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37280050-A-T

101558957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37280075-G-A

101558957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37280075-G-T

101559020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37280105-T-C

101559152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37280206-T-C

101563101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37282204-T-C

101563174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37282270-G-A

101563305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37282381-G-C

101563305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37282381-G-T

101563315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37282391-A-G

101563517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37282554-C-T

101563549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37282577-T-G

101563991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37283170-G-A

101564014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37283193-T-A

101564059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37283230-G-T

101564221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37283380-A-G

101564222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37283381-T-C

101566956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37284416-C-G

101568340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37285198-G-A

101568346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37285204-G-A

101568589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37285435-T-G

101568671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37285904-G-C

http://identifiers.org/hco/8/GRCh38#101568742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37285974-A-C

101568778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37286006-A-T

101568794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37286022-A-G

101568811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37286039-T-C

101569032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37286497-G-A

101569116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37286563-T-A

101570068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37287296-A-G

101570073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37287301-C-G

101570115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37287327-G-T

101573216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37288067-G-A

101573265-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37288101-T-G

101573266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37288102-A-G

101573266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37288102-A-T

http://identifiers.org/hco/8/GRCh38#101573271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37288107-C-A

101573271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37288107-C-T

101573279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37288115-G-T

101573490-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37288261-A-T

http://identifiers.org/hco/8/GRCh38#101573528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37288292-C-A

101573650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37288413-G-C

101573674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: synonymous variant
orthologous variants: 37288438-A-G

101573722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: synonymous variant
orthologous variants: 37288486-G-A

101573963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37288709-G-A

101573963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37288709-G-T

101573983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, undefined
orthologous variants: 37288732-G-A

101573983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, undefined
orthologous variants: 37288732-G-C

101574070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, undefined
orthologous variants: 37288815-C-T

101574073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, undefined
orthologous variants: 37288820-G-A

101574160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37288876-A-G

101574289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37288985-A-G

101574428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37289127-A-G

101574555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37289303-A-G

101574609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, undefined
orthologous variants: 37289356-G-C

101574677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37289445-C-T

101574731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37289495-A-G

101574958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37289771-G-A

101577014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37291226-G-A

101577105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37291303-C-T

101577182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37291381-T-G

http://identifiers.org/hco/8/GRCh38#101577550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37291940-C-A

101577553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37291943-G-A

http://identifiers.org/hco/8/GRCh38#101577619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37291979-A-C

101577619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37291979-A-G

http://identifiers.org/hco/8/GRCh38#101577675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37292042-C-A

101577675-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37292042-C-G

101577706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37292070-C-T

101577724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37292088-A-G

101577869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37292255-A-G

101577972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37292348-A-G

101578067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37292467-G-C

101578154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37292547-T-C

101578384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37292738-C-G

101578446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37292790-G-A

101578450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37292794-G-A

101578450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37292794-G-T

101578641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37292974-C-G

101578641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37292974-C-T

101578822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37293141-C-T

http://identifiers.org/hco/8/GRCh38#101578901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37293229-C-A

101579093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37293419-A-T

101581172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37295906-G-A

101581546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37296212-G-C

101581606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37296261-A-G

101583286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37297016-C-T

101583292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37297022-G-A

101583436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, undefined
orthologous variants: 37297121-C-T

101583472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, undefined
orthologous variants: 37297148-G-A

101583570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, undefined
orthologous variants: 37297219-G-A

101583676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37297319-A-G

101583676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37297319-A-T

101583980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37297561-A-T

101584031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37297584-A-G

101584133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37297661-A-T

http://identifiers.org/hco/8/GRCh38#101585412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37298929-C-A

101585577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37299075-T-A

101585957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37299436-T-A

101586300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37299578-A-G

101586362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37299639-C-G

101586362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37299639-C-T

101586376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37299653-A-G

101586376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37299653-A-T

101587121-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37300682-T-G

101587158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37300707-C-T

101587581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37301162-A-G

101588200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37301436-A-G

101588286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37301499-T-C

101588327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37301562-T-G

http://identifiers.org/hco/8/GRCh38#101588413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37301646-C-A

101588413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37301646-C-T

101588421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37301654-A-G

101588743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37301901-C-G

101588743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37301901-C-T

http://identifiers.org/hco/8/GRCh38#101588747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37301903-C-A

101588860-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37302027-T-A

101589107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37302268-A-G

101589107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37302268-A-T

101589149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37302311-T-C

101589269-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37302432-T-G

101589313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37302470-A-G

101589557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37302777-T-A

101590363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37304163-G-T

101590594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37304333-T-C

101590688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37304404-T-C

101590690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37304406-T-C

101590876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37304596-G-A

101590876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37304596-G-T

101591407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37305138-C-T

101591570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37305299-G-A

http://identifiers.org/hco/8/GRCh38#101591963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37305670-C-A

101596018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307303-G-T

101596107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307354-A-G

101596115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307362-G-A

101596120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307367-A-G

101596259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307396-C-T

101596355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307443-C-T

101596414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307478-T-G

101596422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307489-C-T

101596510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307572-A-G

101596545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307600-A-G

101596617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307701-G-A

101596676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307766-G-A

http://identifiers.org/hco/8/GRCh38#101596703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37307794-A-C

101596755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307831-A-G

101596811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307890-T-G

101596824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37307903-C-G

http://identifiers.org/hco/8/GRCh38#101598937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37309142-A-C

101598938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37309143-T-C

101598938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37309143-T-G

101599106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: synonymous variant
orthologous variants: 37309958-A-G

101599106-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: synonymous variant
orthologous variants: 37309958-A-T

101599170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37310017-T-C

http://identifiers.org/hco/8/GRCh38#101599202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37310049-A-C

101599237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37310106-G-A

101599237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37310106-G-T

http://identifiers.org/hco/8/GRCh38#101599265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37310131-C-A

http://identifiers.org/hco/8/GRCh38#101599679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37310371-C-A

101600508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37311156-C-T

101602265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37312139-A-G

101602338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37312182-C-T

101602420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37312220-G-T

http://identifiers.org/hco/8/GRCh38#101603451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37313054-C-A

101603451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37313054-C-G

101603460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37313063-A-G

101603588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37313188-G-A

101603707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, undefined
orthologous variants: 37313351-A-G

101603738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, undefined
orthologous variants: 37313364-A-G

101603845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37313443-A-G

101604013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37313714-T-A

101604013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37313714-T-C

101604057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37313745-T-G

101604145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37313813-A-G

101604373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37314005-C-T

101604658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37314266-G-T

http://identifiers.org/hco/8/GRCh38#101605049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37315122-A-C

101605095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37315169-C-T

101605293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37315287-A-G

http://identifiers.org/hco/8/GRCh38#101605342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37315328-A-C

101605385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37315348-A-G

http://identifiers.org/hco/8/GRCh38#101605471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37315430-C-A

101605471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37315430-C-G

101605495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37315451-A-T

101605575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37315512-G-A

101605615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37315552-G-A

101605678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37315604-G-T

101605779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37315713-G-A

101605928-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37315891-G-C

101606088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37316039-G-A

101606093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37316044-G-A

101606692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37316585-G-C

101606693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37316586-A-G

http://identifiers.org/hco/8/GRCh38#101606883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37316752-C-A

101606946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37316822-T-C

101607016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37316888-A-T

101607112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37316975-T-A

101607410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37317874-T-C

101607553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37317962-T-A

101607741-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37318150-T-A

101608136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, undefined
orthologous variants: 37318549-G-A

101608322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37318714-G-A

101608499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37318852-C-T

101610038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37320529-C-T

101610598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37320946-C-T

101611924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37321661-C-T

101612313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37321724-G-A

101612416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37321828-A-T

101612506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37321879-T-C

101612506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37321879-T-G

101612607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37321928-A-T

101613259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37322523-A-G

101613263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37322527-A-G

101613360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37322620-A-G

101613457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37322700-C-T

101613570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37322786-G-A

101614765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37324137-T-G

101614789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37324160-A-G

101614940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37324293-T-C

http://identifiers.org/hco/8/GRCh38#101615056-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37324402-A-C

101615369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37324701-A-G

101615769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37325086-T-C

101615945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37325254-G-A

101616556-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37325389-C-G

101616557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37325390-T-C

http://identifiers.org/hco/8/GRCh38#101616581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37325414-C-A

101617007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37325788-C-T

101617311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37326191-T-C

101617384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37326256-A-G

101617466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37326328-C-G

101617466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37326328-C-T

101617714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37326575-A-G

http://identifiers.org/hco/8/GRCh38#101617725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37326586-A-C

101617800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37326641-C-T

101617828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37326662-G-A

101618622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37327718-C-T

101618774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37327841-C-G

101618810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37327873-G-A

101619411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37328350-A-G

101619521-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37328456-T-G

101619750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37328685-T-C

101619791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37328726-G-T

101619795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37328730-T-C

101619818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37328751-A-G

101619829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37328762-G-A

101619829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37328762-G-T

101619870-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37328800-T-G

101619876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37328806-G-T

101620252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37329152-A-G

101620335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37329204-G-A

101620386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37329253-A-G

101624738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37331092-A-G

http://identifiers.org/hco/8/GRCh38#101625355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37331289-A-C

101629812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37334072-C-T

101629872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37334121-T-C

101629896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37334145-A-G

101630186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37334345-T-A

101630219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37334362-C-T

101630457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37334560-A-G

101630633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37334741-A-G

101630700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37334794-G-A

101630788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37334858-G-A

101631554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37335810-T-A

http://identifiers.org/hco/8/GRCh38#101631778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37336090-C-A

101631778-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37336090-C-G

101631821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37336134-G-A

101631821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37336134-G-T

http://identifiers.org/hco/8/GRCh38#101631830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37336143-C-A

101632094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37336311-T-A

101632097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37336314-T-C

101632219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 37336443-C-T

101632350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37336574-G-C

101632372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 37336596-C-T

101632398-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37336619-C-G

101632398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37336619-C-T

101632841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37336976-A-G

101633214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37337290-A-G

101633232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37337308-A-G

http://identifiers.org/hco/8/GRCh38#101633330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37337393-A-C

101633383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37337443-T-G

101633453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37337498-T-C

101633813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37337808-C-T

101633894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37337879-T-C

101636812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37337945-T-C

101636942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37338065-T-G

101636944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37338067-C-G

101637021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37338137-T-A

101637021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37338137-T-C

101637053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37338165-T-A

101637244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37338313-T-C

101637331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37338378-C-T

101637382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37338425-C-T

101637650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37338616-C-T

101638120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37339622-G-A

101638151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37339653-T-C

101638251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37339738-T-A

101638251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37339738-T-C

101638336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37339849-C-T

101638394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37339987-A-G

101638396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37339989-T-C

101638441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37340035-G-T

101638470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37340070-A-G

101638924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37342177-C-G

101639296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37342498-G-A

101639353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37342576-T-C

101639538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37342762-C-T

101639578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37342796-A-G

101639675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37342900-C-T

101642133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37343453-A-G

101642337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37343655-G-T

http://identifiers.org/hco/8/GRCh38#101642668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37343972-C-A

101644140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37344906-C-G

101644140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 37344906-C-T

101644241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345017-G-A

101644243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345019-G-A

101644243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345019-G-T

http://identifiers.org/hco/8/GRCh38#101644278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37345048-C-A

101644335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345094-G-A

101644335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345094-G-T

101644510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345198-T-C

101646446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345542-A-G

101646447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345543-T-C

101646731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37345759-T-C

http://identifiers.org/hco/8/GRCh38#101647005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37346017-C-A

101647879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346563-G-T

101647880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346564-A-T

101647958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346653-G-A

http://identifiers.org/hco/8/GRCh38#101648103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37346836-A-C

101648269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37346993-G-A

101648293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347017-T-C

101648503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347217-G-A

http://identifiers.org/hco/8/GRCh38#101648522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37347236-C-A

101648522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347236-C-T

101648653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347326-C-T

101648741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347378-T-C

101648789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347408-G-A

101648994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347576-G-A

101648994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347576-G-T

101649062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347644-G-A

http://identifiers.org/hco/8/GRCh38#101649304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37347885-C-A

101649304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347885-C-T

101649305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347886-G-A

101649305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347886-G-T

http://identifiers.org/hco/8/GRCh38#101649326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37347905-C-A

http://identifiers.org/hco/8/GRCh38#101649329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37347909-C-A

101649366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347961-A-T

http://identifiers.org/hco/8/GRCh38#101649381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37347982-C-A

101649381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37347982-C-T

http://identifiers.org/hco/8/GRCh38#101649402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37348001-C-A

101649402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37348001-C-T

http://identifiers.org/hco/8/GRCh38#101649523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37348126-C-A

101649523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37348126-C-T

101649532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37348135-A-G

http://identifiers.org/hco/8/GRCh38#101649582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37348183-C-A

101649582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37348183-C-T

http://identifiers.org/hco/8/GRCh38#101649703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37348281-A-C

101651333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37350589-G-A

101651563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37350803-T-C

101651913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351106-A-G

101651946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351139-C-T

101652267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351368-C-T

101652278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351382-T-A

101652287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351391-G-A

101652287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351391-G-T

101652542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351733-T-G

101652547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351737-G-T

101652554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351744-A-G

101652554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351744-A-T

101652557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351747-T-G

101652559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351749-T-G

101652561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351751-G-A

101652561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351751-G-C

101652561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351751-G-T

101652562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351752-T-C

101652562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351752-T-G

101652574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351761-G-T

101652577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351764-G-A

101652587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351774-T-G

101652598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351786-G-C

101652598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351786-G-T

101652619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351811-T-C

101652785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37351981-T-C

http://identifiers.org/hco/8/GRCh38#101652839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37352025-C-A

101652992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37352217-A-G

101653614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37352736-G-T

101653883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37352827-C-T

101653960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37352876-T-G

101654243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37353164-C-T

http://identifiers.org/hco/8/GRCh38#101654495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37353371-C-A

101654527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37353403-A-G

101654590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37353513-A-T

101654614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37353667-G-T

101654765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37353810-C-T

101662426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37356563-T-A

101662468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37356595-T-A

101662678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37356753-G-A

101662776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37356839-A-G

101663195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37357223-C-T

101663745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37357579-G-A

101664409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37358570-G-A

101664410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37358571-G-A

101664556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37358706-A-G

http://identifiers.org/hco/8/GRCh38#101664564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37358714-C-A

http://identifiers.org/hco/8/GRCh38#101664846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37358924-A-C

101664846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37358924-A-G

101665207-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37359305-T-G

http://identifiers.org/hco/8/GRCh38#101665532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37359666-C-A

101665532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37359666-C-T

101665686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37359986-G-A

http://identifiers.org/hco/8/GRCh38#101665803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37360089-A-C

101666520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37360907-G-A

101666520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37360907-G-T

101666661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 37361053-G-A

101666771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37361160-C-T

http://identifiers.org/hco/8/GRCh38#101666807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37361200-A-C

101667010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37361388-G-A

101667010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37361388-G-T

http://identifiers.org/hco/8/GRCh38#101667100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37361486-C-A

101667100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37361486-C-T

101667130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37361512-A-G

101667285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37361667-G-A

101667285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37361667-G-T

http://identifiers.org/hco/8/GRCh38#101667287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37361669-C-A

101667287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37361669-C-T

101667331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37361714-T-A

http://identifiers.org/hco/8/GRCh38#101667440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37361815-A-C

101667535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37361896-G-T

101667606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37361953-C-T

101667634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37361979-T-C

101667719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362051-T-C

101667782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362112-A-G

http://identifiers.org/hco/8/GRCh38#101667868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37362197-C-A

101667868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362197-C-T

101667869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362198-G-A

101667869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362198-G-T

101667905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362235-G-A

101667905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362235-G-T

101668000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362295-C-G

101668025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362311-G-A

101668025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362311-G-T

101668160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362401-A-G

101668233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362484-G-A

101668233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362484-G-T

101668374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362636-T-C

101668454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362706-A-G

101668478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362730-G-A

101668478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362730-G-T

http://identifiers.org/hco/8/GRCh38#101668584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37362829-C-A

101668584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362829-C-T

101668638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362877-T-C

101668658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362897-T-C

101668721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37362955-T-C

http://identifiers.org/hco/8/GRCh38#101668855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37363067-C-A

101668855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37363067-C-T

http://identifiers.org/hco/8/GRCh38#101668856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37363068-C-A

101668856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37363068-C-T

101668933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37363118-G-A

101668933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37363118-G-T

101669130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37363275-G-T

http://identifiers.org/hco/8/GRCh38#101669302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37363402-C-A

101669302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37363402-C-T

101669348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37363439-T-C

101669348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37363439-T-G

http://identifiers.org/hco/8/GRCh38#101669385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37363478-C-A

http://identifiers.org/hco/8/GRCh38#101669426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37363519-C-A

101669426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37363519-C-T

101669591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37363681-T-A

101669762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37363847-G-A

101669798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37363880-G-T

http://identifiers.org/hco/8/GRCh38#101669854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#37363925-C-A

101669854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37363925-C-T

101669881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37363952-C-T

101669935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37364020-G-A

101669976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37364059-C-T

101670493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2799
most severe consequence: intron variant
orthologous variants: 37364418-G-T