88803589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 5 prime UTR variant
orthologous variants: 78703122-T-C

http://identifiers.org/hco/15/GRCh38#88803590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78703123-C-A

88803590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 5 prime UTR variant
orthologous variants: 78703123-C-T

88803607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 5 prime UTR variant
orthologous variants: 78703139-G-A

88803607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 5 prime UTR variant
orthologous variants: 78703139-G-C

88803607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 5 prime UTR variant
orthologous variants: 78703139-G-T

http://identifiers.org/hco/15/GRCh38#88803691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78703238-C-A

88803691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 5 prime UTR variant
orthologous variants: 78703238-C-T

88803941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78703481-G-A

88803941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78703481-G-C

88803949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78703490-G-A

88803949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78703490-G-T

88803968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78703505-C-T

88804084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78703611-T-A

88804118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78703630-G-A

88804388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78703889-T-A

88804397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78703898-A-G

http://identifiers.org/hco/15/GRCh38#88804610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78704042-C-A

88804697-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78704107-T-A

88804747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78704156-C-T

88804785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78704196-C-G

88804921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78704340-G-A

88804932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78704351-G-A

88805754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78705003-A-G

http://identifiers.org/hco/15/GRCh38#88806052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78705239-C-A

88806738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78705580-A-T

88806746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78705588-C-G

http://identifiers.org/hco/15/GRCh38#88806846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78705663-C-A

88806846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78705663-C-T

http://identifiers.org/hco/15/GRCh38#88806956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78705766-C-A

88806956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78705766-C-T

http://identifiers.org/hco/15/GRCh38#88807001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78705804-A-C

88807095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706039-T-C

88807235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706198-G-A

88807235-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706198-G-C

88807263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706226-A-G

88807413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706324-T-C

88807695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706539-G-A

88807800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706661-C-G

88807800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706661-C-T

88807918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706776-G-A

88807933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706791-G-A

88807964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706822-A-G

88807976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706834-T-C

88808019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706874-T-A

88808036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706880-G-A

88808046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706890-G-A

88808048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706892-G-A

88808048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78706892-G-T

88808214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78707050-G-C

88808214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78707050-G-T

88808701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78707495-C-G

88808703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78707497-G-A

88808723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78707517-G-C

88808867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78707649-G-A

88808893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78707675-A-T

88809001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78707751-T-A

http://identifiers.org/hco/15/GRCh38#88809275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78708006-C-A

88809275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78708006-C-T

88809373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78708156-C-G

88809474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78708236-G-A

http://identifiers.org/hco/15/GRCh38#88809532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78708282-C-A

88809993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78708694-C-G

88810241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78708940-A-G

http://identifiers.org/hco/15/GRCh38#88810283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78709283-C-A

88810283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78709283-C-T

88810606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78709610-G-T

http://identifiers.org/hco/15/GRCh38#88810701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78709698-C-A

http://identifiers.org/hco/15/GRCh38#88810757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78709751-C-A

88810929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78709853-G-T

88811140-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78710092-G-C

http://identifiers.org/hco/15/GRCh38#88811269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78710179-A-C

88811441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78710520-A-G

http://identifiers.org/hco/15/GRCh38#88811456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78710563-C-A

88811460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78710565-C-G

88811524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78710653-G-A

88811524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78710653-G-C

88811542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78710671-T-C

88811653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78710758-C-T

88811772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78710846-G-C

88811901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78710952-G-A

88812008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78711069-G-T

88812062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78711130-C-G

88812062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78711130-C-T

88812093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78711179-G-A

88812307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78711371-A-G

88812318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78711382-A-G

88812327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78711391-C-T

88812338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78711402-G-A

88812379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78711447-A-G

88813311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78712357-C-G

88813411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78712457-A-G

88813413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78712459-G-A

88813696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78712722-G-A

88813714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78712739-C-T

88813736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78712765-G-A

http://identifiers.org/hco/15/GRCh38#88813820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78712853-A-C

http://identifiers.org/hco/15/GRCh38#88813995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78712996-C-A

88814202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78713485-A-T

http://identifiers.org/hco/15/GRCh38#88814206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78713489-C-A

88814254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78713537-C-T

88814274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78713557-C-T

88814550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78713789-T-C

88814579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, undefined
orthologous variants: 78713815-G-A

88814579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, undefined
orthologous variants: 78713815-G-C

88814589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78713825-C-T

88814597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78713833-A-G

88814705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78713949-C-G

http://identifiers.org/hco/15/GRCh38#88814706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78713950-C-A

88814706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78713950-C-T

88814903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78714144-T-A

88814957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78714199-G-C

http://identifiers.org/hco/15/GRCh38#88815058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78714279-C-A

88815227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78714415-G-A

http://identifiers.org/hco/15/GRCh38#88815231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78714419-C-A

http://identifiers.org/hco/15/GRCh38#88815361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78714491-C-A

88815361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78714491-C-T

88815433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78714536-C-T

88815713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78714574-G-T

88815800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78714654-G-C

88815809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78714663-T-C

88815966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78714816-T-C

88816419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78715186-T-C

http://identifiers.org/hco/15/GRCh38#88816702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78715434-C-A

88816707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78715439-A-G

88816884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78715581-A-G

88817030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78716074-C-G

88817030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78716074-C-T

88817085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78716131-C-T

88817919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78716381-C-T

88818046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78716491-G-C

88818196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78716636-G-A

88818276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78716719-T-C

88818503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78716910-C-T

http://identifiers.org/hco/15/GRCh38#88818746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78717123-C-A

88819238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78718250-G-A

88819397-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78718395-C-G

88819397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78718395-C-T

88819398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78718396-G-A

88819398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78718396-G-C

88819653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78718704-C-T

88819763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78718886-C-T

http://identifiers.org/hco/15/GRCh38#88819807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78718993-A-C

88819851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78719028-G-A

88819851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78719028-G-C

88819890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78719060-C-T

88819903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78719073-G-A

88819912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78719088-G-A

88819913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78719089-A-T

88820213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78719553-A-G

88820299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78719638-G-A

88820357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78719699-C-T

88821496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78720056-G-A

88821549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78720090-C-T

88821764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78720315-G-T

88822119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78720392-C-G

88822134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78720407-C-G

http://identifiers.org/hco/15/GRCh38#88822185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78720459-C-A

http://identifiers.org/hco/15/GRCh38#88822286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78720569-C-A

88822288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78720571-G-C

88822425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78720687-C-T

88822848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78720823-T-A

88822848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78720823-T-C

88823158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78721116-C-G

88823247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78721206-C-T

http://identifiers.org/hco/15/GRCh38#88823254-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78721213-A-C

88823259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78721218-T-C

88823260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78721219-T-G

88823737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78721658-G-C

88823767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78721687-G-C

88823822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78721701-G-T

88823870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78721749-A-G

88823897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78721774-T-C

88823903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78721780-C-T

88823965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78721830-G-A

http://identifiers.org/hco/15/GRCh38#88824040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78721892-C-A

88824784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78722293-C-G

88824784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78722293-C-T

88824804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78722329-G-A

88824804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78722329-G-T

88824907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78722438-A-G

88824993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78722510-T-C

88825158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78722669-A-G

88825266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78722842-C-T

88825278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78722854-G-C

88825629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78723161-T-C

88825777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78723267-C-T

88825799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78723290-A-G

88827076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78724042-C-G

88827356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78724277-A-G

88827450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78724338-T-C

88827539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78724357-T-C

88827591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78724374-T-C

88827601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78724384-A-G

http://identifiers.org/hco/15/GRCh38#88827618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78724401-A-C

88827673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78724454-G-A

88827716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78724489-G-A

88827779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78724570-C-T

88827840-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78724627-T-A

88827971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78724763-C-T

88828141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78725185-G-C

88828161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78725205-G-T

88828250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78725308-T-A

88828437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78725477-C-T

88828459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78725493-G-A

88828459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78725493-G-C

88828567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78725597-A-G

88828772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78725775-T-A

88828772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78725775-T-C

http://identifiers.org/hco/15/GRCh38#88828788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78725843-C-A

88828820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78725875-G-A

88828820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78725875-G-C

http://identifiers.org/hco/15/GRCh38#88829047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78726254-C-A

88829126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726336-G-A

88829196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726403-T-A

88829196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726403-T-C

88829285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726541-G-A

88829285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726541-G-T

88829298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726572-T-A

88829298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726572-T-C

88829400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726656-G-A

88829435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726692-T-A

88829435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726692-T-G

88829503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726737-C-T

88829542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726776-C-T

88829554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726788-C-T

88829560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726794-T-G

88829638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726870-A-T

88829718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78726939-G-A

88829830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78727050-C-T

88829842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78727062-G-C

88829886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78727093-C-T

88829905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78727112-G-A

88831107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78727277-C-G

88831145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78727316-A-G

88831209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78727380-G-C

88831330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78727487-A-G

88831538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78727734-T-C

88831725-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78728010-T-G

http://identifiers.org/hco/15/GRCh38#88831786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78728071-C-A

http://identifiers.org/hco/15/GRCh38#88831906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78728169-C-A

88831906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78728169-C-T

88831924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78728186-A-T

88832661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78728918-T-C

88832665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78728922-C-T

http://identifiers.org/hco/15/GRCh38#88832758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78729013-C-A

http://identifiers.org/hco/15/GRCh38#88833361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78729661-C-A

88833438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78729740-C-T

88833530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78729823-C-T

88833711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78729997-C-G

88833714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78730000-C-T

88833761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78730025-T-A

88833800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78730065-G-A

88834102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78730350-C-G

88834169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78730420-G-T

88834254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78730494-G-A

88834319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78730549-G-A

88834440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78730658-C-T

88834568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78730786-T-C

88834629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78730863-C-G

88834757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78730968-A-G

http://identifiers.org/hco/15/GRCh38#88834968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78731124-C-A

88835523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78731395-A-G

88835716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78731529-C-T

http://identifiers.org/hco/15/GRCh38#88836063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78731827-C-A

88836063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78731827-C-T

88836108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78731873-G-T

http://identifiers.org/hco/15/GRCh38#88836122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78731883-C-A

88836122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78731883-C-T

http://identifiers.org/hco/15/GRCh38#88836160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78731911-C-A

88836160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78731911-C-T

88836310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78732046-A-G

88836332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78732063-G-C

88836334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78732065-G-A

http://identifiers.org/hco/15/GRCh38#88836344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78732078-C-A

88836344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78732078-C-G

88836344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78732078-C-T

88836582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78732268-T-A

88837034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78732466-G-A

88837118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78732504-C-T

88837427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78732698-G-T

http://identifiers.org/hco/15/GRCh38#88837429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78732700-C-A

88837529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78732793-G-A

88837835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78733095-G-A

88837868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78733128-G-A

88838041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78733253-A-G

88838119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78733328-C-T

88838196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78733389-G-A

88838207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78733403-A-G

http://identifiers.org/hco/15/GRCh38#88838259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78733918-C-A

88838321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78733980-T-C

88838423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78734059-A-G

88838445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78734080-G-A

88838516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78734115-A-G

88838554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78734120-G-A

88838554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78734120-G-T

http://identifiers.org/hco/15/GRCh38#88838564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78734130-C-A

88838564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78734130-C-G

88838564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78734130-C-T

88838673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78734225-C-T

88838707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78734259-C-G

88838850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78734402-G-A

http://identifiers.org/hco/15/GRCh38#88839009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78734561-C-A

88839009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78734561-C-T

88839039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78734591-G-A

http://identifiers.org/hco/15/GRCh38#88839080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78734630-A-C

http://identifiers.org/hco/15/GRCh38#88839124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78734676-C-A

http://identifiers.org/hco/15/GRCh38#88839162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78734734-C-A

88839162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78734734-C-T

88839244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78734859-C-G

88839272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78734927-C-T

88839353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78735222-G-A

http://identifiers.org/hco/15/GRCh38#88839428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78735297-C-A

88839477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78735344-A-G

http://identifiers.org/hco/15/GRCh38#88839839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78735624-C-A

88839839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78735624-C-T

88839875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78735809-A-G

88839891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78735915-G-A

88839895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78735919-A-G

http://identifiers.org/hco/15/GRCh38#88840194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78736192-C-A

88840194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 78736192-C-T

88840222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78736234-G-A

88840222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78736234-G-C

88840432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78736422-C-T

88840542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78736645-C-T

88840601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78736704-G-A

88840644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78736743-A-G

88841401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78737595-G-T

88841416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78737617-C-T

88841592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78737780-A-G

88841592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78737780-A-T

88841593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78737781-G-A

88841593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78737781-G-T

http://identifiers.org/hco/15/GRCh38#88841629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78737815-A-C

88841629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78737815-A-G

88841664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78737852-G-A

88841717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78737903-C-T

http://identifiers.org/hco/15/GRCh38#88841904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78738071-C-A

http://identifiers.org/hco/15/GRCh38#88841907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78738074-C-A

88841907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738074-C-T

88841933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738098-T-C

88841959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738125-G-A

http://identifiers.org/hco/15/GRCh38#88841991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78738160-C-A

88841991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738160-C-T

88842002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738171-T-C

88842002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738171-T-G

88842087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738248-A-G

88842087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738248-A-T

88842119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738276-A-G

88842239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738398-C-T

88842256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738419-C-G

88842256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738419-C-T

88842260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738423-A-G

88842309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738486-C-G

88842309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738486-C-T

88842312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738489-G-A

88842783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738829-C-T

88842944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78738979-G-T

88843231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739237-G-A

88843231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739237-G-T

88843245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739249-G-A

88843245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739249-G-C

88843274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739266-G-A

88843274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739266-G-T

88843293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739285-G-A

88843293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739285-G-C

88843293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739285-G-T

88843296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739288-G-A

88843296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739288-G-C

88843296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739288-G-T

http://identifiers.org/hco/15/GRCh38#88843324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78739316-A-C

88843324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739316-A-G

88843324-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739316-A-T

88843356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 78739352-T-A

88843356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 78739352-T-C

88843356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 78739352-T-G

88843678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739677-T-A

88843784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739741-G-C

88843784-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739741-G-T

88843849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739784-T-C

88844931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78739934-G-T

88845396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78740594-G-A

http://identifiers.org/hco/15/GRCh38#88845498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78740680-C-A

88845603-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78740785-C-G

88845650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78740832-T-C

http://identifiers.org/hco/15/GRCh38#88845653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78740835-C-A

88845653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78740835-C-T

88845684-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78740866-C-G

88845684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78740866-C-T

http://identifiers.org/hco/15/GRCh38#88845821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78741012-C-A

88846250-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78741246-C-G

88846250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78741246-C-T

88846370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78741368-T-C

88846442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78741436-A-G

88846458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78741460-A-G

88846499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78741501-A-G

http://identifiers.org/hco/15/GRCh38#88846919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78741795-C-A

88846919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78741795-C-G

88846954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78741825-A-G

http://identifiers.org/hco/15/GRCh38#88846967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78741838-C-A

88846967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78741838-C-T

88847047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78741891-C-T

88847120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78741955-T-C

http://identifiers.org/hco/15/GRCh38#88847185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78741999-C-A

88847185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78741999-C-G

88847185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78741999-C-T

http://identifiers.org/hco/15/GRCh38#88847238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78742056-C-A

88847238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 78742056-C-T

http://identifiers.org/hco/15/GRCh38#88847247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78742065-C-A

88847247-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78742065-C-G

88847247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78742065-C-T

http://identifiers.org/hco/15/GRCh38#88847317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78742135-C-A

88847317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78742135-C-G

88847317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78742135-C-T

88847328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78742146-G-A

88847328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78742146-G-T

http://identifiers.org/hco/15/GRCh38#88847442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78742263-C-A

88847503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742308-T-C

88847503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742308-T-G

88847508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742313-A-G

88847512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742317-A-G

88847566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742324-A-G

http://identifiers.org/hco/15/GRCh38#88847635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78742373-C-A

88848050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742566-A-G

88848081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742591-G-C

88848081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742591-G-T

88848102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742598-G-C

88848128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742631-C-T

88848156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742647-C-G

88848156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742647-C-T

88848159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742650-T-C

88848159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742650-T-G

88848174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742665-G-A

88848174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742665-G-T

88848179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742670-G-A

88848179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742670-G-C

88848179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742670-G-T

88848298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742771-G-A

88848307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78742780-G-A

88848926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78743181-A-G

88848957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78743212-T-C

88848991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78743224-C-T

88849044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78743281-T-C

http://identifiers.org/hco/15/GRCh38#88849207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78743452-C-A

88849207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78743452-C-T

88849240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78743484-G-C

88849333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78743581-T-C

88849383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78743651-T-C

88849383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78743651-T-G

88849406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78743675-G-A

88849406-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78743675-G-C

88849406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78743675-G-T

http://identifiers.org/hco/15/GRCh38#88849431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78743723-C-A

88849431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 78743723-C-T

http://identifiers.org/hco/15/GRCh38#88849432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78743724-C-A

88849432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 78743724-C-T

88849460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78743752-C-G

88849464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78743756-G-A

88849464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: stop gained
orthologous variants: 78743756-G-T

http://identifiers.org/hco/15/GRCh38#88849502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78743794-A-C

88849502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78743794-A-G

88849502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78743794-A-T

88849529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78743821-G-A

88849529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78743821-G-C

88849529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78743821-G-T

88849601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78743893-C-T

88849628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78743920-T-C

http://identifiers.org/hco/15/GRCh38#88849679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78743971-C-A

88849679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78743971-C-G

88849682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78743974-G-A

http://identifiers.org/hco/15/GRCh38#88850041-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78744058-A-C

88850081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78744097-T-C

88850108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78744109-G-A

88850114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78744115-G-C

88850249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78744204-T-C

http://identifiers.org/hco/15/GRCh38#88850277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78744232-C-A

88850279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78744234-A-G

http://identifiers.org/hco/15/GRCh38#88850285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78744240-C-A

http://identifiers.org/hco/15/GRCh38#88850917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78745448-C-A

88850917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745448-C-T

88850936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745467-T-A

88850936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745467-T-C

88851100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745589-G-A

88851100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745589-G-T

88851123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745612-G-T

88851167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745830-G-A

88851167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745830-G-C

88851167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745830-G-T

88851179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745842-A-G

88851179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745842-A-T

88851225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745888-G-C

88851225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745888-G-T

http://identifiers.org/hco/15/GRCh38#88851258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78745926-C-A

88851258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745926-C-T

88851259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745927-G-A

88851259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745927-G-T

88851286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745955-T-A

88851286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745955-T-C

88851290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745959-C-T

88851327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78745993-T-C

88851399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78746045-T-C

88851459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78746095-T-C

88851459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 78746095-T-G

88851573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78746188-G-T

http://identifiers.org/hco/15/GRCh38#88851610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78746223-C-A

http://identifiers.org/hco/15/GRCh38#88851737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78746363-C-A

88851737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78746363-C-G

88851741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78746365-G-A

88851752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78746376-G-A

88851752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78746376-G-T

http://identifiers.org/hco/15/GRCh38#88851827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78746448-A-C

88851834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78746455-C-T

88852014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78746611-G-A

88852014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78746611-G-C

88852045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78746641-T-A

88852045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78746641-T-C

88852045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78746641-T-G

88852105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78746715-G-A

88852105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78746715-G-T

88852109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78746719-G-A

88852109-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78746719-G-C

88852109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78746719-G-T

88854291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78747054-C-T

http://identifiers.org/hco/15/GRCh38#88854296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78747059-C-A

88854713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78747383-A-G

http://identifiers.org/hco/15/GRCh38#88854737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78747406-C-A

88854737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78747406-C-G

88854737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78747406-C-T

88854800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78747447-T-G

http://identifiers.org/hco/15/GRCh38#88855165-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78747669-A-C

88855168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78747672-T-C

http://identifiers.org/hco/15/GRCh38#88855318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78747822-C-A

88855374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78747875-G-T

88855394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78747895-C-G

88855394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78747895-C-T

88855418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78747919-G-C

88855442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78747949-G-T

88855521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78748031-G-T

88856854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78748653-C-T

88856885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78748681-T-C

http://identifiers.org/hco/15/GRCh38#88856967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78748763-C-A

88856967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78748763-C-T

88856968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78748764-C-T

http://identifiers.org/hco/15/GRCh38#88857078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78748646-C-A

88857078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78748646-C-T

88857085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78748653-C-T

88857261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78748763-C-T

88857262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78748764-T-C

88857450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78748952-C-T

88857453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78748955-G-A

88857631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78749133-A-G

88857631-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78749133-A-T

88857650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78749152-G-A

88857650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78749152-G-C

88857696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78749198-G-A

88857759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78749261-T-G

88857785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78749287-G-T

http://identifiers.org/hco/15/GRCh38#88857818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78749320-A-C

88857818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78749320-A-T

http://identifiers.org/hco/15/GRCh38#88857828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78749330-A-C

88857842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78749401-A-G

88857922-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78749481-C-G

88857922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78749481-C-T

88857985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78749544-A-G

88858198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78749757-G-A

88858212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78749771-G-A

88858348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78749907-A-G

88858423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78749982-C-T

88858656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78750215-C-T

88858681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78750240-A-G

88858699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78750258-T-A

88858779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78750338-A-T

88858802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78750361-G-T

88858856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78750415-G-A

88858856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78750415-G-T

88858915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78750471-G-C

88859131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78750696-A-G

88859182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78750747-C-T

88859213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78750778-G-T

88859267-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78750832-C-G

88859267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78750832-C-T

88859389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78750954-G-C

88859401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78750966-A-G

88859468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751022-G-A

http://identifiers.org/hco/15/GRCh38#88859472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78751026-A-C

88859591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751128-G-C

88859617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751144-T-C

88859694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751220-T-C

88859697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751223-G-A

88859816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751316-T-C

88859847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751346-G-A

88859880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751374-A-G

88859936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751431-T-C

88860117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751578-C-T

88860128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751589-G-T

88860173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751637-G-A

http://identifiers.org/hco/15/GRCh38#88860186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78751650-A-C

88860186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751650-A-G

88860197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751668-A-G

88860197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751668-A-T

88860201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751672-A-G

http://identifiers.org/hco/15/GRCh38#88860249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78751720-C-A

88860288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751762-G-C

88860288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751762-G-T

http://identifiers.org/hco/15/GRCh38#88860293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78751767-C-A

88860293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751767-C-G

http://identifiers.org/hco/15/GRCh38#88860352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78751802-C-A

88860352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, missense_variant
orthologous variants: 78751802-C-T

88860359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, missense_variant
orthologous variants: 78751809-G-A

88860359-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, missense_variant
orthologous variants: 78751809-G-C

88860359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, missense_variant
orthologous variants: 78751809-G-T

http://identifiers.org/hco/15/GRCh38#88860451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78751884-A-C

88860451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78751884-A-G

http://identifiers.org/hco/15/GRCh38#88860456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78751889-C-A

88861418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78752092-C-T

88861686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78752362-A-G

88862766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78752502-G-A

88862768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78752504-C-T

88862801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78752557-C-T

88863009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78752758-A-G

88863030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78752863-T-A

88863031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78752864-G-A

88864876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78754538-T-C

88864885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78754547-T-A

88865071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, undefined
orthologous variants: 78754702-T-C

88865119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78754746-C-T

88865122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78754749-G-A

88865506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78755012-A-G

http://identifiers.org/hco/15/GRCh38#88865545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#78755053-A-C

88865549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, undefined
orthologous variants: 78755057-A-T

88865625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78755111-C-G

88865660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78755143-C-T

88865669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78755152-T-G

88865697-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78755233-T-G

88865878-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, undefined
orthologous variants: 78755567-A-T

88866285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78755908-C-G

88866417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78756055-G-A

88866487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78756125-G-A

88866487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78756125-G-T

88866602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78756226-T-C

88866796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78756389-G-T

88866875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78756460-G-A

88866894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78756480-C-G

88866894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78756480-C-T

http://identifiers.org/hco/15/GRCh38#88867247-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78756879-C-A

88867344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78756977-G-A

88867344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78756977-G-T

88867464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78757089-C-T

88867475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78757100-G-C

88868110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78757765-A-G

88868111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78757766-G-T

88868114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78757768-G-A

88868114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78757768-G-T

88868158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78757812-G-A

88868158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78757812-G-T

88868184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78757831-G-A

88868184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78757831-G-T

88868335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78757982-G-A

88868335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78757982-G-T

88868365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758012-T-C

88868392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758035-T-A

88868416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758059-G-A

88868416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758059-G-T

http://identifiers.org/hco/15/GRCh38#88868452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78758094-C-A

88868452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758094-C-T

88868490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758138-A-G

88868836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758531-G-A

88868838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758533-G-A

88868838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758533-G-T

88868910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758603-A-G

88868958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758652-T-C

88869117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758794-G-A

88869167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758842-C-G

88869167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78758842-C-T

88869650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78759287-C-G

88869685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78759325-G-T

http://identifiers.org/hco/15/GRCh38#88869797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78759421-C-A

88869817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78759441-C-T

88869911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78759538-T-G

88869944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78759562-C-T

88870074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78759683-T-C

88870254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78759842-G-A

88870356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78759968-C-G

88870362-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78759974-G-C

88870511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78760127-T-G

88870543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78760157-G-A

88870586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78760191-G-A

88870927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78760521-A-G

88871042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78760618-C-T

88871086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78760664-C-G

88871086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78760664-C-T

88871194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78760756-A-G

88871302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78760872-C-T

http://identifiers.org/hco/15/GRCh38#88871356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78761016-C-A

88871362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761022-G-T

88871442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78761102-C-T

88871475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78761135-G-A

88871475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense variant
orthologous variants: 78761135-G-T

88871482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78761142-G-A

http://identifiers.org/hco/15/GRCh38#88871617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78761272-C-A

88871617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761272-C-T

88871626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761312-G-T

88871627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761313-C-G

88871627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761313-C-T

88871647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761403-G-A

88871647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761403-G-T

88871794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761523-G-A

88871869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761598-G-T

http://identifiers.org/hco/15/GRCh38#88871873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78761602-C-A

88871873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761602-C-T

88871909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761626-T-A

88871965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761667-G-A

88871965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761667-G-T

88871982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761685-A-T

88872151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761829-A-G

88872155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761833-A-G

88872155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761833-A-T

http://identifiers.org/hco/15/GRCh38#88872158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78761836-C-A

88872158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761836-C-T

http://identifiers.org/hco/15/GRCh38#88872188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78761863-C-A

88872207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761894-C-G

88872207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761894-C-T

88872214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78761901-G-T

88872447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762121-T-G

http://identifiers.org/hco/15/GRCh38#88872750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78762286-A-C

88872750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762286-A-G

88872768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762304-T-A

88872768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762304-T-C

88872768-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762304-T-G

88872790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762325-T-A

88872790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762325-T-C

http://identifiers.org/hco/15/GRCh38#88872833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78762373-C-A

http://identifiers.org/hco/15/GRCh38#88872866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78762407-C-A

88872866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762407-C-T

88872946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78762487-G-A

88873009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78762550-G-A

88873009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78762550-G-C

88873009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: synonymous variant
orthologous variants: 78762550-G-T

88873057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762598-G-A

88873057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762598-G-T

88873079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762617-A-G

http://identifiers.org/hco/15/GRCh38#88873081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78762619-A-C

88873081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762619-A-G

88873106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762644-G-A

88873106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762644-G-T

88873107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762645-G-C

88873107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762645-G-T

88873131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762669-G-A

88873131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762669-G-T

http://identifiers.org/hco/15/GRCh38#88873362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78762899-C-A

88873420-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762956-C-G

88873420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78762956-C-T

88873556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78763090-C-T

88873588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78763127-T-C

http://identifiers.org/hco/15/GRCh38#88873594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78763133-C-A

88873594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78763133-C-G

88873594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78763133-C-T

88873669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78763207-G-A

88873669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78763207-G-C

88873669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron variant
orthologous variants: 78763207-G-T

88873737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78763278-G-A

88873737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78763278-G-C

88873737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78763278-G-T

88873808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 78763368-A-G

88873837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 78763398-C-G

88873960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78763521-C-T

88874002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78763563-G-T

88874007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78763568-A-G

88874048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78763610-G-A

88874048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78763610-G-T

88874102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78763667-G-A

88874103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78763668-G-C

88874103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78763668-G-T

http://identifiers.org/hco/15/GRCh38#88874122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78763688-A-C

88874122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78763688-A-G

88874122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78763688-A-T

88874400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78763941-C-T

http://identifiers.org/hco/15/GRCh38#88874452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78763995-C-A

88874452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78763995-C-T

88874781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78764329-C-T

88874857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3 prime UTR variant
orthologous variants: 78764411-A-G

88874885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3 prime UTR variant
orthologous variants: 78764439-G-T

88874897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3 prime UTR variant
orthologous variants: 78764450-G-A

88874897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3 prime UTR variant
orthologous variants: 78764450-G-T

http://identifiers.org/hco/15/GRCh38#88874906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78764459-C-A

88874906-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3 prime UTR variant
orthologous variants: 78764459-C-G

88874906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3 prime UTR variant
orthologous variants: 78764459-C-T

88874944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3 prime UTR variant
orthologous variants: 78764510-G-A

88874944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3 prime UTR variant
orthologous variants: 78764510-G-T

88875029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3 prime UTR variant
orthologous variants: 78764598-G-A

88875029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3 prime UTR variant
orthologous variants: 78764598-G-T

http://identifiers.org/hco/15/GRCh38#88875183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#78764683-C-A

88875183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 319
most severe consequence: 3 prime UTR variant
orthologous variants: 78764683-C-T