98134679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42507269-G-A

98134679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42507269-G-C

98134679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 42507269-G-T

http://identifiers.org/hco/10/GRCh38#98134739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42507330-A-C

98134774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42507365-T-C

http://identifiers.org/hco/10/GRCh38#98134792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42507382-A-C

98134839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42507432-G-A

98134839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42507432-G-C

98134839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42507432-G-T

98134851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42507444-C-T

98135141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42507730-G-A

98135146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42507735-C-T

98135147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42507736-C-T

98135401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42508000-G-A

98135462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42508046-T-C

98135462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42508046-T-G

98135529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42508111-C-G

98135537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42508119-G-A

98135537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42508119-G-T

98137771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42508853-A-G

98138284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42509719-A-G

98138310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42509742-T-C

98138354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42509763-C-G

98138362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42509771-G-T

98138363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42509775-C-G

98138384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42509797-T-C

98138389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42509803-G-A

98138389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42509803-G-T

98138397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42509812-C-T

98138832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42510126-T-C

98139078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42510347-G-A

98139369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42510596-G-A

98139439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42510667-T-C

98139475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42510691-T-C

98139475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42510691-T-G

98139507-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42510720-T-A

http://identifiers.org/hco/10/GRCh38#98139620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42510818-A-C

98139664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42510861-A-G

98139842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42511028-T-C

98140022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42511237-C-G

98140581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42511702-G-C

98140609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42511730-T-A

98140697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42511811-A-G

98140815-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42511922-C-G

98140815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42511922-C-T

http://identifiers.org/hco/10/GRCh38#98140892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42512003-C-A

98140982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42512091-T-C

http://identifiers.org/hco/10/GRCh38#98141006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42512113-A-C

http://identifiers.org/hco/10/GRCh38#98141189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42512299-A-C

98141278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42512368-A-G

98141381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42512473-T-C

98141408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42512500-T-C

98141416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42512508-G-A

98142254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42513228-T-C

98142349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42513304-C-T

98145133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42513724-T-C

98145201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42513770-T-A

98145201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42513770-T-C

98145367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42513881-T-A

98151256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42514369-G-C

98151256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42514369-G-T

98151434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42514532-G-C

98151664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42514635-C-T

98154803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42515325-C-T

http://identifiers.org/hco/10/GRCh38#98154818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42515339-A-C

98154935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42515392-A-G

98155050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42515482-G-A

98155103-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42515533-T-G

98155448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42515873-A-G

98155473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42515900-C-G

98155618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42516060-A-G

98155651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42516093-T-C

98156053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42516359-T-A

98162655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518339-T-C

98162670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518354-G-C

98162670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518354-G-T

98162678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518362-G-A

98162700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518388-G-A

98162700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518388-G-C

98162719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518407-A-T

98162835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518513-G-A

98162835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518513-G-C

98162835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518513-G-T

98162993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518596-T-A

98162993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518596-T-C

98163005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518611-G-A

98163005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518611-G-T

http://identifiers.org/hco/10/GRCh38#98163062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42518650-C-A

98163063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518651-C-T

98163361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42518943-G-A

98163361-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42518943-G-C

98163361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42518943-G-T

98163369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42518951-T-C

98163414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518988-T-C

98163414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518988-T-G

98163415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518989-A-G

98163415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42518989-A-T

98163503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42519041-T-C

98164077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42519535-G-A

98164476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42520180-G-A

98164868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42520571-G-T

98164916-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42520625-A-T

98165498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42521105-A-G

98167344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42522727-C-G

98167371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42522761-T-G

98167653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42522944-T-A

98167653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42522944-T-C

98167653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42522944-T-G

98168033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42523281-C-T

98168167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42523414-T-C

98168287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42523528-C-G

98168483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42523722-C-T

98168518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42523744-G-T

98169193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42524217-G-A

98169193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42524217-G-T

98169194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42524218-T-G

98169304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42524320-G-A

98169918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42525777-T-G

http://identifiers.org/hco/10/GRCh38#98169971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42525829-A-C

98169984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42525842-G-A

98169984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42525842-G-T

98170014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42525871-G-A

98170795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42526333-A-G

http://identifiers.org/hco/10/GRCh38#98170977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42526478-C-A

98171505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42527058-C-T

98171645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42527192-G-A

http://identifiers.org/hco/10/GRCh38#98171737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42527478-A-C

98171737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42527478-A-T

98173145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42528839-G-A

98173151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42528845-G-A

98173205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42528897-T-A

98173255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42528949-G-A

98173333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42529034-A-G

98173333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42529034-A-T

98173535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42529235-A-G

98173722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42529420-C-T

98173776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42529474-T-C

98173871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42529568-A-G

http://identifiers.org/hco/10/GRCh38#98174021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42529742-A-C

98174223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42530147-T-G

http://identifiers.org/hco/10/GRCh38#98174271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42530194-A-C

98174728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42530946-G-A

98174743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42530961-A-G

98187450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42532415-T-A

98188834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42533439-C-G

98189061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42533648-A-G

98189410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42533972-G-A

98189473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42534019-A-G

98189504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42534042-C-T

98189654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42534236-G-C

98190415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42534559-A-G

98195610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42538774-G-T

98195704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42538908-C-T

98195770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42538976-T-G

98196229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42539601-A-G

98197303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

98197538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42540375-G-A

98197548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42540386-T-G

98198185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42541272-G-A

98198659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42541735-C-T

98198726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

98198821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42541835-C-G

http://identifiers.org/hco/10/GRCh38#98198854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42541868-C-A

98199112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42542115-A-G

98199166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42542170-A-G

98199214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42542214-G-A

http://identifiers.org/hco/10/GRCh38#98199305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42542307-C-A

98200750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42546402-T-G

98200799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42546449-G-A

98201095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42546659-A-G

98203948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42547785-C-G

98204087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42547910-G-C

98204462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42548269-T-A

98204978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42548442-T-C

98205553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42548975-T-A

98205572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42548994-A-G

98205573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42548995-T-C

98205586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 42548998-A-G

98205665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42549074-T-C

98205792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42549188-T-C

98206253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42549813-C-G

http://identifiers.org/hco/10/GRCh38#98206283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42549843-C-A

98206348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42549903-C-T

98208093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 42550983-T-C

98208194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42551084-G-T

98208234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42551124-T-C

98208258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42551148-A-G

98208312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42551196-G-A

98208312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42551196-G-T

98208332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42551219-T-C

98208403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42551290-T-C

98208403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42551290-T-G

98208428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42551321-G-A

98208428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42551321-G-T

98208533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42551426-T-G

98208546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42551439-G-A

98208546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42551439-G-T

98208596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42551489-T-C

98208833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42551711-G-A

98208879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42551757-A-T

http://identifiers.org/hco/10/GRCh38#98208891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42551769-C-A

98208897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42551775-C-G

98208897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42551775-C-T

http://identifiers.org/hco/10/GRCh38#98209002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42551877-A-C

98209002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42551877-A-G

98209085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42551981-C-G

98209085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42551981-C-T

98209112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42552008-G-C

98209130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42552023-C-T

http://identifiers.org/hco/10/GRCh38#98209229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42552122-C-A

98209229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42552122-C-G

98209229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42552122-C-T

http://identifiers.org/hco/10/GRCh38#98209239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42552132-A-C

98209239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42552132-A-G

98209265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42552158-C-T

98209304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42552194-T-C

http://identifiers.org/hco/10/GRCh38#98209383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42552273-C-A

98209383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42552273-C-T

98209399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42552289-A-G

98209411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42552301-G-A

http://identifiers.org/hco/10/GRCh38#98209489-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42552379-A-C

98209489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42552379-A-G

98209810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42552691-C-T

98209836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42552717-G-A

http://identifiers.org/hco/10/GRCh38#98209919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42552800-C-A

98209919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42552800-C-T

98209922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42552803-G-A

98210026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42552933-T-C

98210083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42552986-C-T

98210601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42553450-T-G

98210790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42554172-A-G

98210805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42554187-G-A

98211136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42554488-C-T

98211161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42554512-G-A

http://identifiers.org/hco/10/GRCh38#98211224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42554583-C-A

98211224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42554583-C-G

98211251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42554610-T-C

98211352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42554693-A-G

http://identifiers.org/hco/10/GRCh38#98211386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42554726-A-C

98211496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42554823-G-A

98211496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42554823-G-C

98211496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42554823-G-T

98211518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42554845-T-C

98211746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42555024-G-A

http://identifiers.org/hco/10/GRCh38#98211904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42555163-C-A

98211904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42555163-C-G

98211987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42555240-A-G

98212108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42555338-G-A

98212406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42555584-T-C

98212531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42555702-A-T

98212790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42556155-A-G

98212907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42556251-T-A

98213043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42556349-C-T

98213191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42556494-C-G

98213191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42556494-C-T

98213595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42557018-A-G

http://identifiers.org/hco/10/GRCh38#98213820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42557159-C-A

http://identifiers.org/hco/10/GRCh38#98224248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42560106-C-A

98224320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42560163-C-T

98224678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42560474-A-G

98224730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42560694-A-G

98224730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42560694-A-T

98225283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42561445-G-T

http://identifiers.org/hco/10/GRCh38#98225330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42561477-A-C

98225330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42561477-A-G

98225647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42562081-T-A

98225781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42562213-T-A

98225781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42562213-T-G

98225798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42562230-A-G

98226174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42562304-T-C

http://identifiers.org/hco/10/GRCh38#98226305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42562449-A-C

98226305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42562449-A-G

98226305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42562449-A-T

http://identifiers.org/hco/10/GRCh38#98226312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42562459-C-A

http://identifiers.org/hco/10/GRCh38#98227125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42563279-A-C

98227152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42563293-G-T

98227402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42563500-A-G

98227502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42563630-T-C

98230938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42563798-T-C

98231201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42564049-A-G

98231317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42564276-T-C

98231391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42564345-G-A

98231391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42564345-G-T

98231452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42564402-T-G

98231568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42564521-C-T

98231571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 42564524-T-A

98231571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 42564524-T-C

98232389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42567394-C-G

98232581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42567575-T-C

98232980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42568332-T-C

98233220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42568719-T-G

98233844-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42569776-A-T

98233853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42569791-T-C

98233854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42569792-A-T

98233858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42569796-T-A

98234240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42570193-G-A

98234255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42570208-G-A

98234429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42570342-G-T

98234501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42570414-T-C

98234529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42570441-T-C

http://identifiers.org/hco/10/GRCh38#98234566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42570480-A-C

98234566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42570480-A-G

98234843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42570739-C-T

98235275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42571109-T-C

98235279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42571113-T-G

98235321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42571170-T-C

98235387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42571237-A-G

98235492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42571331-A-G

98235492-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 42571331-A-T

98235590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42571431-G-A

98235590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42571431-G-T

98235615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42571456-A-G

98236049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: synonymous variant
orthologous variants: 42571867-T-C

98236291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42572101-T-G

98236413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42572177-C-T

98236526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42572304-C-T

98236528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42572306-A-G

98236614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42572395-C-T

98236809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron_variant, undefined
orthologous variants: 42572562-T-C

98237267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42573008-A-G

98237349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42573085-T-G

98237350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42573086-G-T

98237734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42573616-C-T

98237970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42573797-G-C

98238373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42573996-C-T

98238556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42574240-T-C

98238610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42574291-C-G

http://identifiers.org/hco/10/GRCh38#98239000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42574674-A-C

98239009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42574683-C-G

98239012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42574686-A-G

98239012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42574686-A-T

http://identifiers.org/hco/10/GRCh38#98239313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42574940-C-A

98239313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42574940-C-G

98239389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42575033-C-G

98239582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42575228-A-G

98239586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42575232-C-T

98240581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42575862-C-T

98240864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42576136-G-T

98241153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42576405-C-T

98241537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42576763-T-G

98241547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42576773-G-T

98241726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42576933-G-C

98242470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42577368-C-G

http://identifiers.org/hco/10/GRCh38#98242495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#42577382-A-C

98242495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42577382-A-G

98242640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42577512-C-T

98242755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42577612-A-G

98243156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42577988-A-G

98243210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42578037-T-C

98243533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42578489-T-C

98243899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42578818-A-G

98243971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42578921-T-C

98244026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: intron variant
orthologous variants: 42578976-G-T

98244257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579206-G-A

98244422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579348-A-G

98244446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579370-G-A

98244450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579374-G-T

98244597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579527-G-A

98244597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579527-G-C

98244597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579527-G-T

98244652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579574-T-C

98244700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579621-A-G

98244705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579626-A-G

98244708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579630-T-G

98244790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579705-G-A

98244790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579705-G-T

98244836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579750-C-T

98244851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23512
most severe consequence: 3 prime UTR variant
orthologous variants: 42579765-A-G