123070168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40696557-C-T

123070233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40696450-T-C

123070360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40696299-C-T

123070448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40696231-G-A

123070448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40696231-G-T

123070975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40695669-G-A

123071800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40695439-G-T

http://identifiers.org/hco/11/GRCh38#123071986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40695229-A-C

123072001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40695214-C-T

123072009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40695206-G-A

123072009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40695206-G-T

123072085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40695134-T-G

123072131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40695087-G-T

123072699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40694680-G-T

123072712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40694666-T-C

123072972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40694384-G-T

123073308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40694071-G-A

123073308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40694071-G-T

123073697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40693678-C-T

123073727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40693648-G-A

123073763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40693612-T-C

123073807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40693553-G-A

http://identifiers.org/hco/11/GRCh38#123073825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40693535-C-A

123073825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40693535-C-G

123074654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692587-T-C

123074664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692577-A-T

123074673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692570-C-G

123074673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692570-C-T

123074888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692362-T-C

123074894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692356-A-G

123074898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692355-G-T

123074899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692354-T-A

http://identifiers.org/hco/11/GRCh38#123074904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40692349-A-C

123074922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692332-T-A

123074922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692332-T-C

http://identifiers.org/hco/11/GRCh38#123074923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40692331-C-A

123074923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692331-C-G

123074930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692324-G-A

123074930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692324-G-C

123074930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692324-G-T

123075765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40692154-T-C

123076399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40691870-T-G

123076681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40691619-T-C

123076756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40691536-A-G

123076882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40691408-G-T

123077055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40691217-A-G

123077156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40691114-G-C

123077156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40691114-G-T

123077190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40691071-G-C

123077265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40690982-G-C

123077324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40690869-A-G

123077399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40690791-T-C

123077761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40690536-T-C

123077780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40690517-T-C

123077970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40690349-G-A

http://identifiers.org/hco/11/GRCh38#123078104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40690226-C-A

http://identifiers.org/hco/11/GRCh38#123079798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40688459-C-A

123079805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40688452-A-G

http://identifiers.org/hco/11/GRCh38#123079821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40688436-C-A

123083159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40685705-T-C

123083159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40685705-T-G

123083171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40685693-A-G

123083299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40685562-T-A

123083356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40685509-G-T

123083382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40685485-T-A

123083658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 40683844-G-A

123083658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 40683844-G-T

123083944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40683561-G-T

123083986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40683517-C-G

123083998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 40683491-T-A

123083998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 40683491-T-C

123084077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40683412-C-T

123084161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40683340-A-G

123084441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 40682879-A-T

123084529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40682583-A-G

123084529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40682583-A-T

123093672-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40677895-T-G

123093685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40677882-C-T

123093690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40677877-A-T

123093692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40677875-G-T

123093872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40677712-C-G

123094999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40675427-C-G

123095018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40675408-T-C

123095073-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40675359-T-A

123095200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40675244-C-T

123095207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40675237-A-G

123096604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40674576-A-T

123096791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40674390-T-G

123097515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672599-G-T

123097571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672553-C-T

123097659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672478-A-G

123097710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672432-G-T

123097720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672422-A-G

123097725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672417-T-C

123097764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672382-G-A

http://identifiers.org/hco/11/GRCh38#123097773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40672374-C-A

123097773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40672374-C-T

http://identifiers.org/hco/11/GRCh38#123097825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40672322-C-A

123097964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40672173-A-G

123097977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672160-G-T

123098006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672132-G-A

123098006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672132-G-T

123098007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672131-G-A

123098007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672131-G-T

123098047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672087-G-A

123098047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672087-G-T

123098058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672081-T-C

123098058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672081-T-G

123098061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672078-G-A

123098061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672078-G-T

123098063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672076-A-G

123098063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672076-A-T

123098090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672047-G-A

123098090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672047-G-C

123098090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40672047-G-T

123098161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40671981-A-G

123098179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40671963-C-T

123098850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40671245-G-A

123098853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40671242-C-T

123098854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40671241-G-A

123099192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40670896-C-G

123099197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40670891-A-T

http://identifiers.org/hco/11/GRCh38#123099204-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40670882-A-C

123099226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40670863-G-A

http://identifiers.org/hco/11/GRCh38#123099299-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40670790-A-C

123099323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40670766-C-G

123099351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40670735-G-C

123099495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40670607-C-G

123103100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40669503-A-T

123103128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40669476-C-G

123103169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40669436-G-A

123104960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40668619-A-G

123104969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40668610-C-T

123108752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40664775-T-C

123108774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40664750-C-T

123108822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40664709-G-A

123108827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40664704-G-A

123108833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40664698-C-G

123109007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40664679-C-G

123109033-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40664649-T-G

123109035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40664647-G-A

123109165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40664534-A-G

http://identifiers.org/hco/11/GRCh38#123109330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40664219-C-A

123109330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40664219-C-T

123109656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40663942-A-G

123109768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40663822-G-A

123109836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40663754-A-T

123109857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40663733-T-A

123111496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40661817-A-G

123111496-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40661817-A-T

123111739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40661588-G-A

123111772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40661555-T-C

123112232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40660410-G-A

123112306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40660335-T-A

123113500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40659844-G-C

123113500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40659844-G-T

123113506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40659838-T-C

123113559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40659781-G-A

123113685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40659668-C-G

123113796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40659476-G-T

123114109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40659168-T-C

123114156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40659131-T-C

123114344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40658943-A-G

123119399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40658696-T-C

123119583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40658503-A-G

123120033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40658025-G-A

123120341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40657872-T-C

123122554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40655640-G-T

123122884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40655165-C-T

123122897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40655152-A-G

123122915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40655137-A-G

123122998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40655056-C-T

123123671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40654717-G-A

123124019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40654397-G-A

123124019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40654397-G-C

123124732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40653593-A-G

123125433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40653074-C-G

123125442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40653070-T-C

123125455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40653057-C-T

123125485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40653037-C-G

123125551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40653018-C-T

123125563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40653006-T-A

123125563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40653006-T-C

123125575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40652994-C-G

123125575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40652994-C-T

123125603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40652968-T-C

123125811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40652733-G-A

123126101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40651131-A-G

123126345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40650830-T-C

123126346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40650829-G-A

123129934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40648709-A-G

123129944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40648699-C-T

123129948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40648695-A-T

123130354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40647960-G-A

123130754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40647195-T-A

123131324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40646969-T-C

123131399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40646929-G-T

123132360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40645019-T-G

123133488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40644446-G-C

http://identifiers.org/hco/11/GRCh38#123134384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40643914-C-A

123134384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40643914-C-T

123134462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40643834-T-C

123134498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40643798-G-A

http://identifiers.org/hco/11/GRCh38#123135275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40643603-A-C

123135345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40643533-A-G

123136991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40642655-T-C

http://identifiers.org/hco/11/GRCh38#123137457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40642484-C-A

123137457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40642484-C-T

123137497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40642450-C-G

123143124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40638643-T-C

123143256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40638513-G-T

123143273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40638479-G-A

123143286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40638466-T-G

123151675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40637977-C-T

123151723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40637929-T-C

123151729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40637923-G-C

123151816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40637839-T-G

123152660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40637011-G-A

123152873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40636799-A-G

123152892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40636787-G-A

123152908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40636771-C-T

123152976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40636716-G-A

123153130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40636565-C-T

123153269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40636428-T-C

123154028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40635915-G-T

123154057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40635887-G-A

123154589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40635391-G-A

123154891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40635199-T-C

123155392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40635012-G-T

123155647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40634761-T-G

123155876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40634539-T-A

123155876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40634539-T-C

123155954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40634476-T-G

http://identifiers.org/hco/11/GRCh38#123155959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40634471-A-C

123155968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40634462-C-T

123156000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40634432-C-G

123156186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40634256-G-A

123156200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40634242-C-G

123156231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40634211-T-C

123156531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40633934-G-A

123156578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40633887-G-T

123156908-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40633587-C-G

123156943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40633554-A-T

123157012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40633498-G-A

123157012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40633498-G-C

123157251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40633279-T-C

123158007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40632623-A-G

123158023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40632607-C-T

123158628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40631401-G-C

123158651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40631378-C-T

http://identifiers.org/hco/11/GRCh38#123158797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40631244-C-A

123158922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40631142-G-A

123159007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40631057-G-A

123159007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40631057-G-C

123159057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40630660-A-G

123159083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40630634-G-A

123159450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40630098-C-G

123159541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40629999-A-G

123159727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40629790-C-T

123159728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40629789-T-C

123159912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40629627-A-G

123160357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40629473-T-G

123160466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40629372-G-A

123160466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40629372-G-T

123160535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40629296-T-C

123160641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40629184-G-A

123161036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40629123-G-T

123161138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40629049-C-T

123161339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40628868-T-C

123161760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40628776-C-T

http://identifiers.org/hco/11/GRCh38#123162066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40628507-A-C

123162100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40628471-T-C

123162162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40628409-T-C

123162541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40628050-G-A

123162546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40628045-G-A

123163209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40627718-C-T

123163325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40627581-T-C

123163439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40627469-G-A

123163709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40627195-G-A

123164319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40626769-C-T

123164328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40626760-A-G

123164366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40626724-C-T

http://identifiers.org/hco/11/GRCh38#123164368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40626722-C-A

123164711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40626446-T-C

123164771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40626385-T-A

123164832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40626320-T-C

123164899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40626251-T-C

123164932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40626212-A-T

123164955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40625997-T-C

123165269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40625686-G-C

123165343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40625614-T-C

123165867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40624689-A-T

123166026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40624522-T-C

123166168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40623422-C-T

123166492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40623098-C-T

123166655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40622941-A-G

123168023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40621555-G-A

123168187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40621394-C-T

123168255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40621325-T-A

123168549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40621062-G-A

123168806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40620746-A-T

123168915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40620621-G-A

http://identifiers.org/hco/11/GRCh38#123169108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40620432-C-A

123169108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40620432-C-T

123169186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40620355-T-C

http://identifiers.org/hco/11/GRCh38#123169360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40620179-C-A

123172980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40617880-A-G

123172998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40617860-C-G

123173040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40617809-C-G

123173054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40617798-A-G

123173366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40617227-A-G

123173441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40617163-T-A

123173446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40617159-A-G

123173644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40616983-C-T

123174123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40616734-G-C

123174884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40616006-T-A

123175740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40615835-G-A

123176045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40615592-T-C

123176068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40615568-A-G

123176215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40615427-G-C

123176226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40615416-G-C

123176234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40615401-G-C

123176460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40614813-G-A

123176531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40614744-A-G

123176869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40614418-C-T

123177001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40614289-T-C

123177302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40614054-G-A

123180860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40611552-G-A

123181101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40611318-A-T

123182066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40609972-C-G

http://identifiers.org/hco/11/GRCh38#123182284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40609657-C-A

123182284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40609657-C-T

123182371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40609554-G-A

123182371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40609554-G-C

123182581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40609424-G-A

123182581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40609424-G-T

123182615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40609408-T-C

123184512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40608718-C-T

123184567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40608679-C-T

123184792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40608458-A-G

123185228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40607892-G-A

123185313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40607844-C-T

123185430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40607762-G-C

123185446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40607746-A-T

123185454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40607741-C-T

123185489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40607706-C-T

123185791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40607429-T-C

http://identifiers.org/hco/11/GRCh38#123186225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40606546-A-C

123186293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40606480-T-C

123186374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40606418-T-A

123186843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40606239-A-T

123187030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40606053-T-C

123187385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40605683-T-C

123187515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40605550-A-G

123187515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40605550-A-T

123187526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40605539-G-A

123187608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40605458-A-G

123187831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40605236-C-T

123187889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40605177-C-G

123188028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40605036-G-T

123188139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40604941-G-T

http://identifiers.org/hco/11/GRCh38#123188454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40604690-C-A

123188659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40604509-G-T

123188691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40604477-G-A

123188691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40604477-G-T

123188694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40604474-G-A

123188694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, undefined
orthologous variants: 40604474-G-T

123188726-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron variant
orthologous variants: 40604444-T-G

123188862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40604287-G-A

123188862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40604287-G-T

123188991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40604158-G-A

123188991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40604158-G-T

123189095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40604040-T-A

http://identifiers.org/hco/11/GRCh38#123189243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40603937-C-A

123189243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40603937-C-T

123189342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40603850-G-T

123190227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40602458-G-A

123190227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40602458-G-T

123190251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40602434-T-C

123190252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40602433-A-G

123190593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40602142-T-C

123190981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601772-G-A

123190999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601754-G-C

123191196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601562-G-A

123191259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601488-C-T

123191283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601468-G-T

http://identifiers.org/hco/11/GRCh38#123191311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40601440-A-C

http://identifiers.org/hco/11/GRCh38#123191318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40601433-C-A

http://identifiers.org/hco/11/GRCh38#123191334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40601417-C-A

123192246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40601327-A-G

123192509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40600886-C-T

123192510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40600885-G-A

123192577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40600802-A-G

123192580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40600799-G-C

123192837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40600436-A-G

123193283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40599310-G-T

123193368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40599218-A-G

123193699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40598926-G-A

123193741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40598862-C-T

123193805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40598787-A-G

123194429-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40598169-T-G

123194787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40597779-A-G

123194898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40597668-C-G

123194898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 40597668-C-T

123194948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40597621-C-G

123194948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40597621-C-T

123194999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40597571-G-A

123194999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 40597571-G-T

http://identifiers.org/hco/11/GRCh38#123195039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24039
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#40597531-C-A