98943400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47207910-T-C

98943412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47207919-A-G

98943444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47207949-G-A

98943548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47208052-T-A

98943548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47208052-T-C

98943548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47208052-T-G

http://identifiers.org/hco/9/GRCh38#98943571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47208077-C-A

98943571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47208077-C-T

98943706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47208119-T-C

98943793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47208178-G-A

98943793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47208178-G-T

98943854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47208230-G-A

98943854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47208230-G-T

98943880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47208256-G-T

http://identifiers.org/hco/9/GRCh38#98943902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47208276-C-A

98943902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47208276-C-T

http://identifiers.org/hco/9/GRCh38#98943903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47208277-C-A

98943903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 47208277-C-T

98943980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47208327-T-C

98944048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 47208340-C-T

98944102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47208383-C-G

98944106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47208387-G-A

http://identifiers.org/hco/9/GRCh38#98944257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47208541-A-C

http://identifiers.org/hco/9/GRCh38#98944294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47208565-C-A

http://identifiers.org/hco/9/GRCh38#98944330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47208574-C-A

98944330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47208574-C-T

98944469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47208690-G-A

98944469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47208690-G-T

98944489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47208706-G-A

98944669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47208881-G-A

98944807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47209013-C-T

98944843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47209044-G-C

98944855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47209056-C-G

98945044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47209212-T-A

98945096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47209267-C-T

http://identifiers.org/hco/9/GRCh38#98945621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47209630-C-A

98946169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47209920-T-C

98946677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47210432-A-G

98946698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47210459-A-G

98947155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47210927-T-C

98947171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47210943-A-G

98947211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47210983-C-T

98947318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47211062-G-A

98947358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47211102-G-A

98947364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47211108-G-A

98947637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47211364-A-G

http://identifiers.org/hco/9/GRCh38#98947740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47211467-C-A

98947752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47211479-A-G

98947759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47211486-T-A

98947759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47211486-T-C

98947789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47211509-G-A

98947809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47211528-G-A

98948049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47211751-A-T

98948091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47211763-G-A

98951870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47214050-T-A

98952014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47214186-T-C

98952295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47214446-A-G

98952320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47214472-T-A

98952377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47214529-T-C

98952450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47214599-A-T

98952545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47214683-C-T

http://identifiers.org/hco/9/GRCh38#98952970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47215178-C-A

98952970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47215178-C-G

98952970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47215178-C-T

98952992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47215202-A-T

98953099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47215302-G-C

98953439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47215673-C-T

98953476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47215760-A-T

98953511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47215816-A-G

98953551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47215865-T-A

98953551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47215865-T-C

98953562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47215880-C-T

98953778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47216077-T-C

98953803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47216102-T-C

98954026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47216310-C-G

98954115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47216390-C-T

98954130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47216405-T-C

98954175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47216449-A-G

98954611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47217450-C-T

98954715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47217522-C-T

98954852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47217658-A-G

98954883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47217720-C-T

98954984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47217801-T-G

98955000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47217817-G-A

98955341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47218459-C-T

98955430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47218528-T-C

98955539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47218636-G-A

98955539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47218636-G-C

98955824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47218990-C-T

98955853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47219057-A-G

98955997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47219204-T-C

98956421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47220004-A-G

98956817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47220372-G-A

98956995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47220498-G-C

98956995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47220498-G-T

98956999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47220502-T-C

98957004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47220507-C-T

98957036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47220537-G-A

98957060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47220555-C-T

98957163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47220627-C-T

98957205-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47220669-G-C

98958007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47221078-G-A

98958085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47221169-T-C

98958284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47221365-G-A

98958462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47221545-C-T

98958668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47221742-G-C

98958917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47221956-G-A

98958934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47221972-G-A

98962135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47225184-T-G

http://identifiers.org/hco/9/GRCh38#98962153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47225202-C-A

98962153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47225202-C-T

http://identifiers.org/hco/9/GRCh38#98962202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47225255-C-A

98962202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47225255-C-G

98962202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47225255-C-T

98962227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47225285-T-G

98962246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47225301-T-G

98962582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47225569-G-A

98962920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47225910-T-C

98963245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47226258-C-T

98963382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47226346-G-A

98963878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47226802-T-C

98963891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47226814-C-T

98963945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47226882-A-T

98964112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227096-C-G

98964395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227347-C-T

http://identifiers.org/hco/9/GRCh38#98964442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47227394-C-A

http://identifiers.org/hco/9/GRCh38#98964604-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47227567-A-C

98964785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227719-G-A

98964856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227783-A-G

98964940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227872-T-C

98964950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227882-C-T

http://identifiers.org/hco/9/GRCh38#98964985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47227917-C-A

98964985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47227917-C-T

98965382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228250-G-A

98965458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228292-G-A

98965498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228332-T-C

98965513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228347-A-T

98966362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47228986-G-A

http://identifiers.org/hco/9/GRCh38#98966439-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47229063-A-C

http://identifiers.org/hco/9/GRCh38#98966582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47229163-C-A

http://identifiers.org/hco/9/GRCh38#98966684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47229265-C-A

98966685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47229266-C-T

98967004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230070-T-G

98967280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230364-C-G

98967382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230526-C-G

98967424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230579-T-A

98967721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47230866-G-C

98967958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47231056-T-C

98968378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47231404-G-A

98971730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47231830-G-A

98971775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47231875-G-A

98971951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232005-G-A

98972209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232265-C-T

98972429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232417-C-T

98972533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232467-C-T

98973060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47232908-G-A

98973307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233175-G-A

98973334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233202-C-T

98973612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233454-G-A

98973867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47233668-A-G

98974224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47234025-G-A

98974417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47234212-G-A

98974418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47234213-G-A

http://identifiers.org/hco/9/GRCh38#98974676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47234610-C-A

98974676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47234610-C-G

http://identifiers.org/hco/9/GRCh38#98974691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47234630-C-A

98974748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47234668-A-G

98974836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47234733-G-A

98975014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47234924-G-T

98975056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47234985-C-T

98975081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47235019-A-G

98975120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47235058-C-T

98975227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47235167-T-C

98975747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47235625-G-A

98975804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47235699-A-T

98976136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47236351-A-G

98976614-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47236767-G-C

98976979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47236976-C-T

98977272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47237231-C-T

98977520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47237472-G-A

98977532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47237484-G-A

98977534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47237486-C-G

http://identifiers.org/hco/9/GRCh38#98977662-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47237596-C-A

98977680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47237614-G-A

98977826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47237787-G-A

98977900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47237863-G-C

98977985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47237949-C-T

98978125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47238064-T-C

98978438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47238291-A-G

98978513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47238336-C-T

98978606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47238420-A-G

98978606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47238420-A-T

98978626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47238440-C-T

98978638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47238491-T-C

98978824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47238753-G-A

98978841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47238770-C-T

98978879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47238808-C-G

98978879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47238808-C-T

98978903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47238837-C-T

98979305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47239229-G-A

98979461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47239392-A-G

98979478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47239418-G-T

98979554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47239503-A-G

98979726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47239730-T-G

98979853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47239904-T-C

98980199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47239987-T-G

98980249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47240043-A-G

98980289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47240090-T-C

98980391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47240195-T-C

98980502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47240323-C-T

98980507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47240328-G-A

98980680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47240487-G-C

98980686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47240493-G-T

98980717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47240522-G-A

98980796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47240584-C-T

98981755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47241561-A-T

98981802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47241606-A-G

http://identifiers.org/hco/9/GRCh38#98981803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47241607-A-C

98981964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47241733-T-C

98982283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47242049-A-G

98984244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47244379-G-C

98984279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47244417-A-G

98984436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47244520-G-A

98984467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47244553-G-A

98985304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47245125-G-C

98985320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47245151-T-A

98985320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47245151-T-C

98985342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47245172-A-G

98985352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47245182-A-G

98985471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47245287-G-A

98985472-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47245288-T-A

98985557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 47245343-C-T

98985623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47245409-G-A

98986064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 47245850-T-C

98986726-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47246955-G-C

98986827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247059-C-T

98986829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247061-T-G

98986919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247138-G-C

98986987-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247190-A-T

98987143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247341-G-A

98987143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247341-G-T

98987196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247385-T-C

98987197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247386-A-G

98987197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247386-A-T

98987214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247400-G-A

98987214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247400-G-T

http://identifiers.org/hco/9/GRCh38#98987215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47247401-C-A

98987215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247401-C-T

98987235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247421-A-T

98987245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247430-A-G

98987246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247431-T-C

98987246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247431-T-G

98987253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247438-T-C

98987256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247441-G-A

http://identifiers.org/hco/9/GRCh38#98987296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47247478-C-A

98987296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 47247478-C-G

98987368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 47247550-G-A

98987368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 47247550-G-T

http://identifiers.org/hco/9/GRCh38#98987374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47247575-C-A

98987399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47247600-C-G

98988202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47248364-T-C

98988404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47248541-C-T

98989051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47249034-C-G

98989074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47249057-T-C

98989074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47249057-T-G

98989075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47249058-G-A

98989502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47249414-G-T

98989597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47249477-A-G

98989630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, undefined
orthologous variants: 47249498-G-A

98990009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, undefined
orthologous variants: 47249781-A-G

98990095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, undefined
orthologous variants: 47249862-A-G

98990320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47249988-T-C

98990342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47250006-T-C

98990350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47250014-G-C

http://identifiers.org/hco/9/GRCh38#98990354-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47250018-A-C

98990356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47250020-C-G

98990358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47250022-C-T

98990713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47250341-C-G

98990713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47250341-C-T

98992847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47250462-C-T

98992858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47250473-C-T

98992874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47250489-G-A

98993170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47250766-C-T

98993198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47250793-T-C

98993414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47251002-G-T

98993456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47251034-G-C

98993512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47251108-G-A

98993512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47251108-G-C

http://identifiers.org/hco/9/GRCh38#98993610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47251205-C-A

98994011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47251509-A-G

98994118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47251654-T-G

98994444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47251933-G-A

98994647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47252065-C-T

98994756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47252200-T-G

98995104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47252548-A-G

98995207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47252562-C-G

98995208-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47252563-T-G

98996606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47253683-C-G

98996690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47253757-A-G

98996797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47253864-A-G

98996802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47253869-G-T

98996897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47253930-A-G

http://identifiers.org/hco/9/GRCh38#98996914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47253947-C-A

98996928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47253984-C-T

98996999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47254055-G-A

98996999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47254055-G-T

http://identifiers.org/hco/9/GRCh38#98997003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47254059-C-A

98997003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47254059-C-G

98997003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47254059-C-T

98997103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254156-T-C

98997111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254164-G-A

98997122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254175-G-A

98997122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254175-G-T

98997152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254187-T-C

98997361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254345-C-G

98997509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254476-T-C

http://identifiers.org/hco/9/GRCh38#98997573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47254570-A-C

98997647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254624-G-A

98997677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254654-C-T

http://identifiers.org/hco/9/GRCh38#98997742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47254714-C-A

http://identifiers.org/hco/9/GRCh38#98997783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47254758-C-A

98997783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254758-C-G

http://identifiers.org/hco/9/GRCh38#98997795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47254769-C-A

http://identifiers.org/hco/9/GRCh38#98997896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47254866-C-A

98997896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254866-C-T

98997956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254911-G-A

98997997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254937-G-C

98997997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47254937-G-T

98998091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47255026-A-G

98998151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47255054-A-T

98998292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47255165-T-C

98998410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47255278-C-T

98998669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47255503-G-A

98998806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47255653-C-T

98998956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47255790-A-G

98999096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47255907-C-G

98999227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47255990-C-T

98999228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47255991-G-A

99000246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47256537-C-T

99000431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47256712-T-C

99000448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47256732-A-G

99000596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47256877-C-T

99000735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47257055-A-G

99000736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47257056-T-C

99000778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47257099-C-T

99000804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, undefined
orthologous variants: 47257125-G-A

http://identifiers.org/hco/9/GRCh38#99000865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47257186-C-A

99000865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47257186-C-G

99000865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47257186-C-T

http://identifiers.org/hco/9/GRCh38#99000902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47257220-C-A

99000937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47257255-A-G

http://identifiers.org/hco/9/GRCh38#99000971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47257293-C-A

99000971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47257293-C-G

99000971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47257293-C-T

99000975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47257297-T-C

http://identifiers.org/hco/9/GRCh38#99001011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47257307-A-C

99001011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47257307-A-T

99001098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47257373-G-T

99001136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47257399-G-A

99001241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47257483-A-G

99001246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47257488-T-C

99001342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47257567-T-C

99003042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47258230-C-T

99003306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47258503-A-G

99003314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47258511-A-G

99003315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47258512-T-C

99003361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47258559-G-A

99003361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47258559-G-T

http://identifiers.org/hco/9/GRCh38#99003394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47258605-C-A

99003485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47258702-G-A

99003485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47258702-G-T

99003640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47258840-T-C

99003640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47258840-T-G

99003698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47258894-T-C

99003708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47258904-G-A

99003708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47258904-G-T

99003755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47258957-G-A

99003859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47259061-T-C

99004827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47259777-T-C

99004827-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47259777-T-G

99005087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47259997-G-A

99005087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47259997-G-T

99005112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47260015-G-T

99005285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47260189-C-T

99005633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47260500-T-C

99005702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47260568-G-A

99005952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47260798-T-A

99006111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47260930-C-T

99006215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47261003-G-A

http://identifiers.org/hco/9/GRCh38#99006279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47261067-A-C

99006279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47261067-A-G

http://identifiers.org/hco/9/GRCh38#99015279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47262129-C-A

http://identifiers.org/hco/9/GRCh38#99015312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47262164-C-A

99015465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47262313-G-A

99015511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47262482-C-T

http://identifiers.org/hco/9/GRCh38#99015638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47262601-C-A

http://identifiers.org/hco/9/GRCh38#99015721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47262685-C-A

http://identifiers.org/hco/9/GRCh38#99015873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47262838-C-A

99015873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47262838-C-T

99015874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47262839-G-A

99015874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47262839-G-T

99015940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47262904-G-T

99016061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47263010-C-T

99016119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 47263068-A-G

99016146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47263089-G-C

99016146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47263089-G-T

99016243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47263165-A-G

99016417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47263320-A-T

99016977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47263763-G-A

99019608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47266354-G-A

99019624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47266368-C-T

99019643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47266397-G-T

99019772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47266523-A-G

99019787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47266537-C-T

99019792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47266542-C-T

99019933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, undefined
orthologous variants: 47266672-G-A

http://identifiers.org/hco/9/GRCh38#99020008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#47266751-C-A

99020872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47266896-G-C

99020939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47266929-T-C

99021397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47267270-G-C

99021443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47267312-A-G

http://identifiers.org/hco/9/GRCh38#99021539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47267415-C-A

99021539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47267415-C-T

99021575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47267461-G-A

99021707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47267563-C-T

99021710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47267566-C-T

99022256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47267964-G-T

99022290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47267997-G-A

99022485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47268160-T-C

99022513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47268188-T-C

99023205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47268940-T-A

99023205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47268940-T-C

99023205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47268940-T-G

99023302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269010-T-C

99023310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269018-G-A

99023310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269018-G-T

99023361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47269067-G-A

99023371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47269077-A-G

99023463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269169-A-G

99023508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269199-G-A

99023508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269199-G-T

99023509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269200-G-A

99023509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269200-G-T

http://identifiers.org/hco/9/GRCh38#99023587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47269273-C-A

99023587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269273-C-T

99023589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269275-T-C

99023653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269327-G-A

99023744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269412-G-A

99023744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269412-G-C

99023922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269548-G-T

99024050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269704-C-T

99024069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269719-T-C

99024104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269753-C-T

99024143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47269792-C-T

99024682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270079-T-C

99024778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270169-G-T

99024782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270173-G-C

99024782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270173-G-T

99024840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270223-C-G

99024840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270223-C-T

99024879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47270257-T-G

99024882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47270260-A-G

99025030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270408-G-A

99025035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270425-T-C

99025137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270486-A-G

99025147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270496-T-C

http://identifiers.org/hco/9/GRCh38#99025148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47270497-C-A

99025615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270682-G-A

99025615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270682-G-C

99025615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270682-G-T

99025657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270722-A-G

99025796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270811-G-A

99025796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270811-G-T

http://identifiers.org/hco/9/GRCh38#99025822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47270834-C-A

99025840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47270850-G-T

99026035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47271031-A-G

99026047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47271043-G-A

99026050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47271046-T-A

99026050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47271046-T-C

99026443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47271317-C-G

99026646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47271474-C-T

99026681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47271509-G-T

99026915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47272342-C-G

99026924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47272351-T-G

99027182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, undefined
orthologous variants: 47272571-C-T

99027259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47272625-G-C

99027348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47272707-C-T

99027542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47272900-C-T

99027828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47273158-C-G

99027829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47273159-A-G

99027830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47273160-G-A

99028030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47273299-G-A

99028908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47273690-C-T

99029081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47273852-A-G

99029112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47273876-G-A

99029195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47273938-T-A

99029198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47273941-T-C

99029231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47273974-G-C

99029439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47274176-A-G

http://identifiers.org/hco/9/GRCh38#99029441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47274178-A-C

99029519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47274255-C-T

99030074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47274447-C-G

99030479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, undefined
orthologous variants: 47275408-G-A

99030517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47275446-C-T

99030519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47275448-G-A

99031168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47276272-G-A

99031279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47276375-G-A

99031279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47276375-G-T

99031751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47276820-T-C

http://identifiers.org/hco/9/GRCh38#99031777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47276839-A-C

99031875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47276935-A-G

99032029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47277179-C-T

99032675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47277555-T-C

99032715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47277588-T-C

99033220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47278046-A-G

99033630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47278480-G-A

99033630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47278480-G-T

99033750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47278598-A-G

99033750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47278598-A-T

99033962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47278844-C-T

99034229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47279093-G-A

99034532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47279387-G-T

http://identifiers.org/hco/9/GRCh38#99034666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47279490-C-A

99034666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47279490-C-T

99034680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47279504-T-C

99034765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47279588-G-A

99035207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47280005-A-G

99035538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47280311-G-A

99035538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47280311-G-T

99035634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47280353-G-T

99035924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47280571-T-G

99036079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47280754-A-G

http://identifiers.org/hco/9/GRCh38#99036106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47280775-C-A

99036106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47280775-C-T

99036217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47280894-G-A

99036217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47280894-G-T

99036426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47281100-A-G

99036503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47281166-A-T

99036777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47281411-G-A

99036809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47281443-G-C

99036809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47281443-G-T

99038106-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47282007-T-A

99038125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47282025-G-A

99038125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47282025-G-T

99038144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47282044-T-C

99038747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282702-G-A

http://identifiers.org/hco/9/GRCh38#99038752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47282707-C-A

99038752-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282707-C-G

99038752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282707-C-T

http://identifiers.org/hco/9/GRCh38#99038764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47282719-C-A

99038764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282719-C-G

http://identifiers.org/hco/9/GRCh38#99038778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47282733-C-A

99038778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282733-C-T

99038842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282781-T-A

99038854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47282793-G-T

99039150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283058-C-G

99039150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47283058-C-T

99040084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 47283568-C-T

99040469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284444-C-T

99040579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284535-T-C

99040605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284561-A-T

99040650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 47284603-G-A

http://identifiers.org/hco/9/GRCh38#99040830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47285204-C-A

99040869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47285243-C-G

99040869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47285243-C-T

http://identifiers.org/hco/9/GRCh38#99041162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47285498-C-A

99041171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 47285505-A-T

http://identifiers.org/hco/9/GRCh38#99041269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47285597-A-C

99041308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 47285637-A-G

http://identifiers.org/hco/9/GRCh38#99041319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#47285648-C-A

http://identifiers.org/hco/9/GRCh38#99041482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47285793-A-C

99041482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47285793-A-G

99041482-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47285793-A-T

99041562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47285879-G-A

99041562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47285879-G-T

99041745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47286012-G-A

99041786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47286052-G-C

http://identifiers.org/hco/9/GRCh38#99041819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47286084-A-C

99041819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47286084-A-T

99041918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47286821-A-G

http://identifiers.org/hco/9/GRCh38#99042014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47286999-C-A

99042014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47286999-C-T

http://identifiers.org/hco/9/GRCh38#99042119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47287101-C-A

99042119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47287101-C-T

99042254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47287189-G-A

99042254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47287189-G-C

99042259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47287194-T-C

99042770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47287706-T-C

99042788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47287723-A-G

99042835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47287761-C-T

99042984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47287928-T-C

99043014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47287959-A-G

99043107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47288046-G-C

99043120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47288064-T-C

99043351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47288264-G-A

99043440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47288332-C-G

99043440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47288332-C-T

99043540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47288432-C-T

99043721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47288600-A-G

99043829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47288687-A-G

99044002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47288853-G-A

99044002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47288853-G-T

99044099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47288953-T-A

99044422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47289239-T-C

99044462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47289273-C-G

99044573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47289339-G-A

99044595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47289361-C-G

http://identifiers.org/hco/9/GRCh38#99044606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47289372-C-A

99044661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47289427-G-A

99044667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47289433-T-C

99044950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47289737-C-T

99045132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47290148-A-G

99045197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47290232-A-G

http://identifiers.org/hco/9/GRCh38#99045253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47290277-A-C

http://identifiers.org/hco/9/GRCh38#99045561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47290612-C-A

99045870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47290955-T-A

99046198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47291265-A-G

99047308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47291878-A-G

99047401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47291963-T-A

http://identifiers.org/hco/9/GRCh38#99047596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47292142-C-A

http://identifiers.org/hco/9/GRCh38#99047640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47292183-C-A

99047640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292183-C-T

99047644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292187-G-C

99047871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292401-G-A

99047871-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292401-G-C

99047871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292401-G-T

99047883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292412-G-A

99047985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47292514-A-G

99047985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47292514-A-T

http://identifiers.org/hco/9/GRCh38#99048009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47292537-C-A

99048009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292537-C-T

99048059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292611-G-T

99048079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292631-G-A

99048079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292631-G-C

99048079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292631-G-T

99048082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292634-G-T

http://identifiers.org/hco/9/GRCh38#99048116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47292668-C-A

99048116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292668-C-T

http://identifiers.org/hco/9/GRCh38#99048136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47292685-C-A

99048136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292685-C-T

99048139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292688-C-T

99048145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292694-A-G

99048145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292694-A-T

99048195-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292754-T-G

99048248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292815-G-A

99049363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292895-G-A

99049363-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292895-G-C

99049363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292895-G-T

99049425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292956-G-A

99049425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47292956-G-T

http://identifiers.org/hco/9/GRCh38#99049473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47293003-C-A

http://identifiers.org/hco/9/GRCh38#99049719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47293209-C-A

99049719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47293209-C-G

99049719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47293209-C-T

99049774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47293264-G-A

99049840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47293354-C-G

99049930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47293441-T-C

99049974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47293484-G-C

99050248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47293713-A-G

99050628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47294062-C-G

99051079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47294519-G-A

99051121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47294568-C-T

99051224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47294656-C-T

99051394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47294827-G-A

99051681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47295065-G-A

99051812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47295298-G-A

99051835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47295413-C-T

99051840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47295418-C-G

99051840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47295418-C-T

99052028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47295765-G-T

http://identifiers.org/hco/9/GRCh38#99052236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47295953-A-C

99052236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47295953-A-G

http://identifiers.org/hco/9/GRCh38#99052237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47295954-C-A

99052237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47295954-C-T

http://identifiers.org/hco/9/GRCh38#99052501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47296166-C-A

99052501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47296166-C-T

99052535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47296200-G-A

99052535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47296200-G-T

99052585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47296240-G-A

99052585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47296240-G-C

99052593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47296245-C-T

99052679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47296314-A-T

99052787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47296381-C-T

http://identifiers.org/hco/9/GRCh38#99053398-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47297623-A-C

99053522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47297722-G-A

99053563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47297770-C-G

99053696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47297886-G-A

99053704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47297894-C-G

99053815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47297995-T-C

99053863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47298043-C-T

99054298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47298455-G-A

99054325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47298470-A-G

99054396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47298531-T-A

99054396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47298531-T-C

99054428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47298559-T-G

99054429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47298560-G-T

http://identifiers.org/hco/9/GRCh38#99054668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47298767-C-A

99054668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47298767-C-G

99054739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47298784-A-G

99054754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47298799-A-G

99054849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47298919-A-T

99054882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299014-A-G

99054882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299014-A-T

99054920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299051-A-G

http://identifiers.org/hco/9/GRCh38#99054968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47299093-C-A

99054968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299093-C-G

99054980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299109-G-T

http://identifiers.org/hco/9/GRCh38#99054991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47299120-C-A

99054991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299120-C-G

99055015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299143-A-G

99055015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299143-A-T

99055026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299154-G-A

99055026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299154-G-C

99055166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299556-A-T

99055339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47299773-G-A

99055363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47299797-A-G

http://identifiers.org/hco/9/GRCh38#99055430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47299853-C-A

99055430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299853-C-T

http://identifiers.org/hco/9/GRCh38#99055446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47299869-C-A

99055446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299869-C-T

99055504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299931-C-T

http://identifiers.org/hco/9/GRCh38#99055509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47299934-C-A

99055509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47299934-C-T

99055659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47300047-A-G

99055699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47300084-G-A

99055939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47300245-C-G

99055973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47300272-G-A

99056010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47300308-G-C

99056361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47300571-G-A

99056514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47300712-G-A

99056514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47300712-G-T

http://identifiers.org/hco/9/GRCh38#99056552-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47300746-A-C

99056552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47300746-A-G

99056552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47300746-A-T

99057777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47302172-G-C

99058029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47302411-A-G

99058428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47302790-G-A

99058433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47302795-G-T

http://identifiers.org/hco/9/GRCh38#99058487-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47302849-A-C

99058498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47302860-T-G

http://identifiers.org/hco/9/GRCh38#99058837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47302969-C-A

99058876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47303008-T-G

99059701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47303711-C-T

99059835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47303814-G-A

99060962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: -C-T

99061026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: -T-C

99061050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: -C-T

99061077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: -T-C

http://identifiers.org/hco/9/GRCh38#99061193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: -C-A

99061193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: -C-G

99061207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: -C-T

99061219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: -C-T

99061537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: -C-T

http://identifiers.org/hco/9/GRCh38#99061580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: -C-A

99061897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47306648-G-A

99061897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47306648-G-T

99061913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47306664-A-G

99062141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47306885-C-T

99062154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47306898-A-G

99062157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47306901-C-G

99062157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47306901-C-T

99062160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47306905-C-T

99062177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47306922-T-G

99062213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47306932-T-C

http://identifiers.org/hco/9/GRCh38#99062214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47306933-C-A

http://identifiers.org/hco/9/GRCh38#99062316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47307035-C-A

99062402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307093-G-T

99062431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307122-A-G

99062478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307163-C-T

99062526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307200-G-A

99062645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307401-C-T

99062937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307644-G-A

99062937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307644-G-T

http://identifiers.org/hco/9/GRCh38#99063007-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47307707-A-C

99063007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307707-A-T

http://identifiers.org/hco/9/GRCh38#99063011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47307711-C-A

99063011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307711-C-T

99063014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307714-A-G

99063014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307714-A-T

99063064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47307762-G-A

99063064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47307762-G-T

http://identifiers.org/hco/9/GRCh38#99063137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47307835-C-A

99063145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307843-G-A

99063145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307843-G-T

99063164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307861-G-A

99063164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47307861-G-T

99063202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47308096-G-A

99063202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47308096-G-T

http://identifiers.org/hco/9/GRCh38#99063214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47308126-C-A

99063254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47308168-A-G

http://identifiers.org/hco/9/GRCh38#99063531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47308461-A-C

99063835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47308682-C-T

99063959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47308806-G-A

99063975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47308822-C-G

99064090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47308939-G-A

99064113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47308964-C-T

99064363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47309225-A-G

99064382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47309243-T-C

99064801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47309624-G-C

99064817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47309634-G-A

99066476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47310111-C-T

http://identifiers.org/hco/9/GRCh38#99066506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47310157-C-A

http://identifiers.org/hco/9/GRCh38#99066536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47310185-C-A

99066587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47310227-A-G

99066700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47310303-C-T

99066908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47310446-A-G

99067010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47310548-T-C

99067016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47310554-C-T

http://identifiers.org/hco/9/GRCh38#99067046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47310584-C-A

99067046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47310584-C-G

99067046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47310584-C-T

99067095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47310633-T-C

99067138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47310673-T-C

99068575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47310794-T-C

99068615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47310834-A-G

99068615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47310834-A-T

99068687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47310906-G-T

99068698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47310917-T-C

99068704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47310923-G-A

99068704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47310923-G-T

99068709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47310928-A-G

99068722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47310941-G-A

99068722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47310941-G-T

99068788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47310994-G-T

99068818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47311021-G-A

99068818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47311021-G-T

99068874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47311076-C-T

99068985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47311182-G-A

99068985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47311182-G-C

99068986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: intron variant
orthologous variants: 47311183-C-T

99069685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47312089-C-T

99069694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47312098-T-C

99069707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47312111-C-T

http://identifiers.org/hco/9/GRCh38#99069748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47312152-A-C

99069748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47312152-A-G

99069754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47312158-G-A

99069769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47312173-G-A

99069783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47312187-C-T

99069820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47312224-C-T

99069834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: missense variant
orthologous variants: 47312238-G-A

99069847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: synonymous variant
orthologous variants: 47312251-A-G

99069918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312325-A-G

99069976-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312375-T-A

99069976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312375-T-C

http://identifiers.org/hco/9/GRCh38#99070019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47312423-C-A

http://identifiers.org/hco/9/GRCh38#99070081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47312484-A-C

99070081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312484-A-T

99070156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312585-G-A

99070156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312585-G-C

99070156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312585-G-T

99070182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312609-T-G

http://identifiers.org/hco/9/GRCh38#99070224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47312650-A-C

99070224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312650-A-G

99070229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312655-T-C

99070259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312685-T-C

99070303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47312730-T-C

http://identifiers.org/hco/9/GRCh38#99070314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47312741-A-C

99070316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312743-T-A

99070335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312762-C-T

http://identifiers.org/hco/9/GRCh38#99070336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#47312763-A-C

99070336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47312763-A-G

99070648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47313033-T-C

99070746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47313137-T-C

99070747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47313138-G-A

99070747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2192
most severe consequence: 3 prime UTR variant
orthologous variants: 47313138-G-T