http://identifiers.org/hco/8/GRCh38#108606857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43504480-A-C

108606860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43504483-A-T

108606886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43504504-G-T

108606895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43504514-G-T

108607002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43504586-G-T

http://identifiers.org/hco/8/GRCh38#108607016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43504600-C-A

http://identifiers.org/hco/8/GRCh38#108607025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43504609-C-A

108607025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43504609-C-T

108607099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43504686-G-A

108607128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43504714-A-G

108607175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43504762-G-T

108607200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43504783-T-G

108607294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43504858-C-G

108607349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43504910-A-G

108607477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43505465-A-T

108607480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43505468-T-G

108607574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43505562-A-G

108608457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43506677-A-G

108608619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43506841-A-G

108608658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43506884-G-T

http://identifiers.org/hco/8/GRCh38#108608717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43506931-C-A

108608717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43506931-C-T

108609797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43507662-A-G

108609988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43507834-G-A

108609988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43507834-G-T

108609997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43507843-A-G

108610272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43509677-G-A

108610272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43509677-G-C

108610636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43509970-C-G

108610724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43510054-T-A

108610724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43510054-T-C

108610770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43510099-G-C

108611767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43511416-T-C

108612811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43512079-A-G

108612812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43512080-A-G

108613348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43512610-A-G

108613388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43512652-C-T

108613527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43512790-T-C

http://identifiers.org/hco/8/GRCh38#108613770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43513032-C-A

108613770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513032-C-T

http://identifiers.org/hco/8/GRCh38#108613828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43513090-A-C

108613842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513101-A-G

108613927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513178-G-A

108613927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513178-G-T

108614056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513296-G-A

108614056-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513296-G-C

108614056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513296-G-T

108614072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513310-A-T

http://identifiers.org/hco/8/GRCh38#108614081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43513319-C-A

108614081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43513319-C-T

108615187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43514123-C-T

108615617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43514482-T-C

108615803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43514634-T-C

108617310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43515360-A-G

108617413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43515567-A-G

http://identifiers.org/hco/8/GRCh38#108617858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43515997-C-A

http://identifiers.org/hco/8/GRCh38#108618787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43516537-C-A

http://identifiers.org/hco/8/GRCh38#108619389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43518547-C-A

108619389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43518547-C-G

108619475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43518630-G-T

108619478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43518633-T-A

http://identifiers.org/hco/8/GRCh38#108619644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43518779-C-A

108619644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43518779-C-T

http://identifiers.org/hco/8/GRCh38#108619861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43518969-C-A

108619861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43518969-C-T

108619907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43519014-T-C

108619915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43519022-A-G

108620317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43519288-T-C

108622275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43522473-G-C

108622497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43522679-A-G

108622738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43522922-G-A

108622780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43522969-T-C

http://identifiers.org/hco/8/GRCh38#108622842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43523031-C-A

http://identifiers.org/hco/8/GRCh38#108622876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43523057-A-C

108623021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43523182-T-C

108624112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43523650-C-G

108624629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43524775-G-T

http://identifiers.org/hco/8/GRCh38#108624650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43524796-C-A

108624805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43524944-G-T

108624976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43525456-T-G

108625454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43525926-C-T

108625469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43525941-G-A

108625917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43526427-C-T

http://identifiers.org/hco/8/GRCh38#108626318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43526781-C-A

108626468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43526926-T-C

108626538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43526988-T-C

108626597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43527047-G-T

108626715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43527165-C-T

108627303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43527746-C-T

108627546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43527980-C-T

http://identifiers.org/hco/8/GRCh38#108627560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43527994-A-C

108627657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43528088-G-C

108632987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43534635-C-T

108633463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43535082-G-A

108634011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43536838-C-T

108634401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43537218-C-T

108634615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43537369-C-G

108634813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43537538-C-T

108634886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43537610-G-A

http://identifiers.org/hco/8/GRCh38#108635371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43538054-C-A

108635371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43538054-C-T

108635394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43538075-G-A

108635395-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43538076-T-A

108635447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43538123-C-G

108635542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43538227-A-T

108637958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43539879-G-A

108637984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43539904-G-T

108638022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43539942-G-A

108638072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43539987-A-G

108638115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43540030-G-A

108638254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43540166-C-T

108638512-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43540408-T-C

http://identifiers.org/hco/8/GRCh38#108638561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43540455-C-A

108638581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43540467-G-A

108638581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43540467-G-T

108638931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43541212-G-C

108639064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43541336-G-T

108639802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43542097-C-T

108639803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43542098-G-A

108640023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43542299-C-G

108640023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43542299-C-T

108640413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43542832-C-T

108640493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43543274-A-T

108640572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43543338-T-C

108640637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43543403-A-G

108640662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43543426-A-T

108640735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43543487-A-G

108646481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43547778-A-G

108646570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43547870-C-T

108646671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43547956-T-C

108646685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43547971-G-A

108646769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43548055-C-T

108646887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43548166-T-C

108646910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43548189-T-C

108656514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43560808-A-G

108656548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43560842-T-C

108656558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43560852-T-C

108656740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43561018-T-A

108656795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43561063-G-T

108657148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43561413-A-G

108657172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43561437-C-G

108658113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43561979-A-T

108658166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562027-C-T

108658176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562037-G-A

108658259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562119-A-T

108658407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562253-C-T

108658451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562283-G-A

108658719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562527-A-G

108658734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562542-A-G

108658801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562605-G-A

108658801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562605-G-C

108658957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562805-T-G

108659079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562905-T-C

108659093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562923-A-G

108659102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562932-T-C

108659124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43562954-A-G

108659680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43564988-C-T

108659745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43565046-C-G

108659858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43565142-T-A

http://identifiers.org/hco/8/GRCh38#108659910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43565194-C-A

108659922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43565206-C-T

108659937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43565221-C-T

108660045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43565327-C-T

108660358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43565647-G-T

108660503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43565839-C-T

http://identifiers.org/hco/8/GRCh38#108660740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43566063-C-A

108660798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566119-G-C

108660899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566203-G-A

108660958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566243-T-C

108661282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566565-G-A

108661367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566646-C-T

108661374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566653-A-T

108661404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566667-A-G

108661404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566667-A-T

108661450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566713-T-C

108661455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566718-C-T

108661511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43566764-G-C

108662035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567490-G-A

108662062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567517-G-A

108662101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567556-G-A

108662101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567556-G-T

108665089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567773-G-T

108665115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567799-T-G

108665182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43567867-A-G

108665380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568233-T-A

108665444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568295-T-A

108665483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568349-G-T

108665492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568358-T-C

108665630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568496-T-C

108665797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568654-C-T

108665898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568811-T-C

http://identifiers.org/hco/8/GRCh38#108665900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43568813-A-C

108665957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43568993-G-A

108666028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43569067-A-G

108666077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43569131-C-T

108666655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43570039-G-A

108666707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43570086-G-A

108666848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43570247-A-G

108666851-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43570250-T-G

108667115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43570535-T-C

http://identifiers.org/hco/8/GRCh38#108667508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43571054-C-A

108667559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43571106-G-A

108667692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43571259-A-G

108668095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43571607-A-G

108668177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43571688-A-G

108668195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43571706-T-C

108668236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43571799-T-A

108668264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43571866-C-T

108668642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43572407-A-G

http://identifiers.org/hco/8/GRCh38#108668716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43572523-C-A

108668716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43572523-C-T

108668876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43572845-C-T

108668915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43572875-G-A

108668964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43572904-T-C

108669000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43572929-T-C

108669200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43573138-C-T

108669350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43573308-G-A

108669438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43573395-G-T

108669598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43573546-T-C

108669730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43573690-C-G

108670027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43573881-G-A

108670027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43573881-G-C

108670027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43573881-G-T

108670034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43573888-T-A

108670034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43573888-T-G

108670186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43574021-G-A

108670298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43574236-A-G

108670310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43574242-A-G

108670401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43574332-C-T

108671002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43580008-T-C

108671156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43580168-T-G

http://identifiers.org/hco/8/GRCh38#108671230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43580247-A-C

108671271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43580281-A-G

108671313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43580323-C-T

108671410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43580420-G-T

108671861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43580869-G-T

108671894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43580902-G-T

108671899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43580907-G-T

108671974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43580983-T-C

108672509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43581475-G-A

108672594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43581572-T-A

108672748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43581721-A-T

108672833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43581809-G-T

108672975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43581936-T-C

108672975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43581936-T-G

108673074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43582036-A-G

http://identifiers.org/hco/8/GRCh38#108673340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43582643-A-C

108673419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43582709-G-A

108673516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43582806-C-G

108673549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43582837-T-C

108673573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43582861-G-A

108673577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43582865-G-C

108673823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43583057-A-G

108673893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43583128-T-C

108673896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43583131-T-C

108673911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43583146-G-T

108675323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43584301-G-T

108675371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43584349-G-A

108675545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43584528-G-A

108675640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43584626-A-G

108676054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43585058-G-A

108676634-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43594234-A-T

108677106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43594652-T-G

108677113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43594659-C-T

108677122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43594668-G-A

108677247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43594791-C-T

108677303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43594843-A-G

108677331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43594872-C-T

108677626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43595120-T-G

108677942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43595422-A-G

http://identifiers.org/hco/8/GRCh38#108682871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43596917-A-C

108683166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43597198-C-T

108683282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43597312-A-T

108685484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43597593-G-A

108685488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43597597-T-C

108685529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43597630-G-T

108686634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43598724-G-C

108686910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43599009-G-C

http://identifiers.org/hco/8/GRCh38#108688594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43599567-C-A

108688627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43599597-T-C

http://identifiers.org/hco/8/GRCh38#108688780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43599762-C-A

http://identifiers.org/hco/8/GRCh38#108688807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43599789-C-A

108688980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43599953-G-A

108689043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43600016-C-T

http://identifiers.org/hco/8/GRCh38#108689154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43600116-A-C

http://identifiers.org/hco/8/GRCh38#108689246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43600204-A-C

108689331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43600267-A-G

108689331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43600267-A-T

108689333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43600269-G-A

108689466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43600400-G-A

108689714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43600647-T-C

108689714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43600647-T-G

108689909-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43600840-T-A

108689973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43600905-T-C

108690076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43600994-C-T

108690254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43601148-A-T

108690273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43601167-C-G

108690433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43601322-A-G

108690967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43601511-A-G

108690967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43601511-A-T

108691052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43601586-G-A

108691095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43601620-G-T

108691119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43601644-C-T

http://identifiers.org/hco/8/GRCh38#108691150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43601668-A-C

108691250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43601736-A-G

108691250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43601736-A-T

108691317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43601804-C-G

108691317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43601804-C-T

108691486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43602220-G-A

108691486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43602220-G-T

108691493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43602227-C-G

108692068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43613687-C-T

108692159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43613772-T-A

108692205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43613811-C-T

http://identifiers.org/hco/8/GRCh38#108692232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43613839-C-A

http://identifiers.org/hco/8/GRCh38#108692332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43613928-C-A

108692332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43613928-C-T

108692348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43613944-T-C

108692561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43614124-T-C

108692924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43614470-C-T

108693106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43614661-G-A

108693106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43614661-G-C

http://identifiers.org/hco/8/GRCh38#108693452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43614968-C-A

http://identifiers.org/hco/8/GRCh38#108694013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43615483-A-C

108694184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43615536-A-G

108694210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43615562-C-G

108694213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43615565-T-A

108695008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43616141-C-G

http://identifiers.org/hco/8/GRCh38#108695065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43616204-C-A

http://identifiers.org/hco/8/GRCh38#108695124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43616264-C-A

108695124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43616264-C-T

108695356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43616468-G-A

http://identifiers.org/hco/8/GRCh38#108695372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43616484-C-A

108695372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43616484-C-G

108695777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43616841-C-T

108695858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43616907-G-A

108696039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43617003-T-C

108696156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43617119-A-T

108696497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43617437-G-A

108696552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43617492-T-C

108696581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43617520-T-C

108696593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43617532-A-G

108696609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43617548-G-A

108696609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43617548-G-T

108696814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43617720-T-C

108696885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43617780-G-A

108696962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43617840-G-A

108698634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43618236-A-G

108699011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43618821-G-A

http://identifiers.org/hco/8/GRCh38#108699043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43618849-C-A

108699138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43618941-T-C

108699138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43618941-T-G

http://identifiers.org/hco/8/GRCh38#108699140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43618943-C-A

108699145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43618948-T-C

108699194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43618997-T-C

108699206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43619009-T-A

108699206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43619009-T-C

108699209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43619012-C-T

http://identifiers.org/hco/8/GRCh38#108701117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43619568-C-A

108701117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43619568-C-T

http://identifiers.org/hco/8/GRCh38#108701228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43619686-C-A

108701228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43619686-C-G

108701229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43619687-T-A

108701229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43619687-T-C

108701229-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43619687-T-G

108701260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43619714-G-A

108701260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43619714-G-C

108701373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43619825-A-T

108701430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43619882-T-C

108701447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43619900-A-T

108701730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43620177-G-A

108701730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43620177-G-T

http://identifiers.org/hco/8/GRCh38#108701906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43620320-C-A

http://identifiers.org/hco/8/GRCh38#108702006-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43620420-A-C

108702294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43620608-G-A

108702361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43620630-A-G

108702363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43620632-G-A

108702363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43620632-G-T

108702364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43620633-A-G

http://identifiers.org/hco/8/GRCh38#108702376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43620645-C-A

http://identifiers.org/hco/8/GRCh38#108702380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43620649-A-C

108702469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43620738-A-G

108702536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43620803-C-T

108702603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43620869-G-T

108703020-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43621076-T-G

http://identifiers.org/hco/8/GRCh38#108703074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43621128-C-A

108703304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43621302-G-A

108703424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43621385-T-C

108703424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43621385-T-G

108703498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43621464-A-T

108703792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43621704-C-T

108703825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43621737-C-T

http://identifiers.org/hco/8/GRCh38#108704040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43621904-C-A

108704133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43621988-G-T

108704214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 43622061-G-A

http://identifiers.org/hco/8/GRCh38#108704303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43622144-C-A

108704303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43622144-C-T

108704566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43622473-C-T

108704661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43622562-G-C

108704661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43622562-G-T

http://identifiers.org/hco/8/GRCh38#108704798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43622699-C-A

108704947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43626916-G-T

108705098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43627053-T-C

108705203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43627169-G-C

108705225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43627190-A-T

108705269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43627231-C-T

108705322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43627292-C-T

108705585-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43627734-T-G

108705618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43627782-C-T

108705673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43627843-C-T

108705719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43627889-A-G

108705741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43627908-A-T

108705823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43627998-G-A

108705916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43628092-G-T

108706207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43628387-C-T

108706473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43628637-C-G

108718436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43628896-A-G

108718469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43628920-A-G

108718674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43629120-T-A

108718674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43629120-T-C

108719004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43630180-A-G

108719004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43630180-A-T

108719110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43630291-A-G

108719425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43631181-T-C

108719425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43631181-T-G

108719686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43631367-T-A

108719688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43631369-C-G

108719689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43631370-T-G

108719758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43631406-T-C

108720119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43631773-G-A

108720336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43631994-C-T

108720666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43633653-C-T

108721100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43633719-A-G

108721394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43634747-T-G

108721501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43634831-A-G

108721518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43634848-G-A

108721851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43635113-T-C

108722061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43635298-C-T

108722088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43635325-T-G

http://identifiers.org/hco/8/GRCh38#108722698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43635971-A-C

108723011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43636277-A-G

108723029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43636295-T-A

108723050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43636312-C-T

108723962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43637147-T-C

108724066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43637249-C-T

108724067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43637250-G-A

108724084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43637269-C-T

108724172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43637360-T-C

108724233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43637415-A-G

108724294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43637473-C-T

108724354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43637514-T-C

108724435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43637578-T-C

108724492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43637629-C-T

108724509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43637646-G-A

108724645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43637760-T-C

108727532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643126-T-A

108727621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643215-G-A

108727647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643243-G-A

108728081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643636-T-C

108728124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643676-T-C

108728447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43643983-T-C

http://identifiers.org/hco/8/GRCh38#108728477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43644009-C-A

108728668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644199-A-G

108728749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644277-T-C

108728778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644306-G-A

108728802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644319-T-C

108728813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644330-A-G

http://identifiers.org/hco/8/GRCh38#108728840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43644353-C-A

108728840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644353-C-T

108728941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644438-G-T

108729123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644579-G-C

108729153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644607-A-G

108729198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644652-C-G

108729253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644709-T-G

108729296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644752-C-T

108729432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644876-C-T

108729483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644925-T-A

108729541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43644993-C-T

108729589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43645041-G-C

108729801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43645220-T-G

108729852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43645271-G-A

108729870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43645289-A-G

108729912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43645331-G-A

108729912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43645331-G-C

http://identifiers.org/hco/8/GRCh38#108729938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43645362-C-A

108730000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43645423-T-C

108730130-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43645552-T-A

108730485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43645903-A-G

108731103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43647359-T-A

http://identifiers.org/hco/8/GRCh38#108731216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43647454-C-A

108731435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43647653-A-G

108731531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43647749-C-T

108732026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43648201-T-G

http://identifiers.org/hco/8/GRCh38#108732028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43648203-C-A

108734496-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43653880-C-G

108734772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43654137-C-T

108734787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43654152-C-T

108737864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43661347-T-C

108738408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43661797-C-T

108738592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43662014-G-A

108738592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43662014-G-T

108738879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43662310-C-T

108738978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43662443-T-C

108739129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43662602-T-A

108739252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43662711-A-G

http://identifiers.org/hco/8/GRCh38#108739308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43662759-C-A

108743339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43667235-A-G

108743379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43667259-A-G

108743393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43667275-C-T

108743465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43667337-G-C

http://identifiers.org/hco/8/GRCh38#108743696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43667581-A-C

108743896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43667772-G-T

108744087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43667937-C-T

108744259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43668104-T-G

http://identifiers.org/hco/8/GRCh38#108746383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43668747-A-C

108746432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43668796-G-T

108746491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43668847-C-T

108746570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43668926-C-T

108746894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669268-C-T

108746920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669287-T-C

108747132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669486-T-A

108747187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669539-C-G

108747187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669539-C-T

http://identifiers.org/hco/8/GRCh38#108747198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43669549-C-A

108747456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43669787-A-G

108750058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670649-T-C

108750189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670778-G-C

108750229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670818-G-A

108750274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670857-T-C

108750274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43670857-T-G

108751249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671075-C-G

108751252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671078-T-C

108751398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671223-G-A

108751398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671223-G-C

108751421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43671247-C-T

108757572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43698629-A-G

108757719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43699332-A-G

108757833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43699444-C-G

108757964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43699581-A-G

108758043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43699660-T-C

108759808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43708497-G-A

108760731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43709121-G-A

108760929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43709344-G-A

108761452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43709980-A-T

108761618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710145-G-T

108761946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710172-T-C

108761982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710204-A-G

108762016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710235-A-G

108762044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43710263-A-G

108764348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712012-A-G

108764530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712201-A-G

108764726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712410-C-G

108764985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712665-G-A

108765116-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712794-G-C

108765284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43712958-A-G

108765386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713059-G-A

108765412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713085-T-C

108765994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713892-G-A

108766070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43713957-T-G

108766530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43714322-G-A

108766530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43714322-G-T

108766532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43714324-G-C

108769854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43716580-G-A

108770181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43716887-G-A

108770352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43717025-C-T

108770420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43717094-A-G

108770508-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43717177-A-T

108770750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43717408-G-A

108771332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718036-A-G

http://identifiers.org/hco/8/GRCh38#108771439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43718133-C-A

108771439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718133-C-T

108771665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718353-G-A

108771677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718365-T-C

108771690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718378-C-G

108771690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43718378-C-T

108773115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43719075-T-G

108773325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43719288-A-G

108773581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43719529-G-C

108773957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720132-A-T

108773995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720173-T-C

108774104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720282-T-C

108774532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720686-G-C

108774579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720723-C-T

108774632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43720784-C-G

108775507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721495-G-A

108775655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721629-A-G

108775655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721629-A-T

108775726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43721696-C-T

http://identifiers.org/hco/8/GRCh38#108775875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43721848-C-A

108776132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722190-G-T

108776262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722212-G-A

108776824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722620-A-G

108776833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722629-T-C

108777093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722681-T-C

108777133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43722715-A-G

108777647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723055-A-G

108777796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723212-C-T

108778011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723537-T-C

108778030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723605-C-T

108778054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723632-C-T

108778378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43723944-C-T

108778590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724155-G-A

108778713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724263-T-C

108778720-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43724270-C-G

http://identifiers.org/hco/8/GRCh38#108779175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43725203-C-A

108779175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43725203-C-T

http://identifiers.org/hco/8/GRCh38#108779511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43725546-C-A

108779524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43725559-G-A

108779593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43725631-C-T

108779783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43725818-G-A

108779783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43725818-G-T

108779787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43725822-A-G

108780060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43726099-A-G

108780087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43726127-T-A

108780203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43726274-G-A

108780203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43726274-G-C

108780421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43726627-G-C

108780822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43727008-G-A

108780953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43727125-G-A

108781423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43727387-T-C

108781527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43727588-G-A

108782082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43728150-T-C

108782093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43728164-C-T

108782423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43728605-A-G

108782473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43728647-A-G

http://identifiers.org/hco/8/GRCh38#108782610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43728766-C-A

108782922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43729029-C-T

108783034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43729104-T-C

108783037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43729107-G-A

108783038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43729108-T-C

108783212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43729216-T-C

108783774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43729747-T-C

108783774-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43729747-T-G

http://identifiers.org/hco/8/GRCh38#108783793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43729762-C-A

108783830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43729799-G-A

108783830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43729799-G-C

108783830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43729799-G-T

108783897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43729864-T-C

http://identifiers.org/hco/8/GRCh38#108783955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43729921-C-A

108783955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43729921-C-T

108783976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43729941-G-A

108784146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43730095-G-A

108784146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43730095-G-T

108784259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43730202-G-C

http://identifiers.org/hco/8/GRCh38#108784274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#43730217-A-C

108784274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43730217-A-G

108784318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43730261-G-A

108784417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43730360-G-C

108784453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43730396-G-A

108784478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43730421-G-T

108784649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43730592-C-T

108784670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43730613-A-T

108784862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 43730805-A-G

108784862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43730805-A-T

108784885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43730828-G-T

108784903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43730846-A-G

108784981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43730924-G-A

108784981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43730924-G-C

108785186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43731131-G-A

108785186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43731131-G-T

108785302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43731257-T-C

108785333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43731288-A-T

108786219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43732079-C-T

108786311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43732172-A-G

108786481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43732334-T-C

http://identifiers.org/hco/8/GRCh38#108786864-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43732722-C-A

108786865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43732723-C-T

108787091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43732914-G-A

108787170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43732988-T-C

http://identifiers.org/hco/8/GRCh38#108787237-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#43733069-A-C

108787282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733114-C-G

108787282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733114-C-T

108787290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733120-G-A

108787387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733216-G-A

108787399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733228-G-A

108787399-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733228-G-C

108787399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733228-G-T

108787403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43733232-C-T

108787494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43733325-G-A

108787494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43733325-G-C

108787494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43733325-G-T

108787508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43733339-A-G

http://identifiers.org/hco/8/GRCh38#108787510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#43733341-C-A

108787510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26409
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 43733341-C-T