15456851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553223-G-A

15456860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141553214-G-A

15456877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553190-C-G

15456877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553190-C-T

http://identifiers.org/hco/1/GRCh38#15456881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141553186-C-A

15456881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553186-C-G

15456881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553186-C-T

http://identifiers.org/hco/1/GRCh38#15456891-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141553176-C-A

15456892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553175-T-C

http://identifiers.org/hco/1/GRCh38#15456898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#141553169-C-A

15456915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553134-G-C

15456915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553134-G-T

15456928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553121-G-T

15456940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553067-A-T

15456946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553061-G-A

15456946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553061-G-C

15456969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553038-T-A

15456969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553038-T-C

15456969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553038-T-G

15457004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553006-G-A

15457004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553006-G-T

15457009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141553001-G-T

15457028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141552996-G-A

15457042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141552982-G-A

15457072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141552947-T-G

15457094-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141552925-T-A

15457097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141552922-G-A

15457112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141552907-C-G

15461251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549845-G-A

15461301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549805-A-T

15461404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549726-T-G

15461436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549696-T-C

15461436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549696-T-G

15461445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549687-G-A

15461445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549687-G-T

http://identifiers.org/hco/1/GRCh38#15461449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141549683-C-A

15461449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549683-C-T

15461510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549668-G-A

15461553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 141549644-C-T

15461671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549526-C-T

15461682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549521-T-A

http://identifiers.org/hco/1/GRCh38#15461731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141549451-C-A

http://identifiers.org/hco/1/GRCh38#15461737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141549445-C-A

15461737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549445-C-T

http://identifiers.org/hco/1/GRCh38#15461756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141549426-C-A

15461756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549426-C-T

15461780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549399-T-A

15461780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549399-T-C

15461783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549396-G-A

15461783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549396-G-C

15461783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549396-G-T

15461793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549386-G-A

15461793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549386-G-T

15461806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549373-G-T

http://identifiers.org/hco/1/GRCh38#15461821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141549358-C-A

15461821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549358-C-T

15461823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549356-C-T

15461831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549348-T-C

15461835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549344-T-A

15461835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549344-T-C

15461876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549314-G-A

15461884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549306-G-T

15461894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549296-G-T

15461895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549295-G-T

15461899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549291-G-A

15461899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549291-G-T

http://identifiers.org/hco/1/GRCh38#15461928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141549262-C-A

15461928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549262-C-G

15461928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549262-C-T

15461941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549250-G-T

15461943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549248-T-C

http://identifiers.org/hco/1/GRCh38#15461957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141549243-C-A

15461957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141549243-C-T

15462749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141549123-C-T

15462794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141549078-T-C

15462819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141549053-T-C

15462821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141549051-G-A

15462821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141549051-G-T

15462973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141548939-A-G

15462974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141548938-G-A

15462974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141548938-G-C

15462974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141548938-G-T

http://identifiers.org/hco/1/GRCh38#15463058-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141548891-A-C

15463058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron variant
orthologous variants: 141548891-A-G

http://identifiers.org/hco/1/GRCh38#15463159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141548879-C-A

15463270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron variant
orthologous variants: 141548858-A-G

15463270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron variant
orthologous variants: 141548858-A-T

15463349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron variant
orthologous variants: 141548806-A-G

http://identifiers.org/hco/1/GRCh38#15463372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141548785-C-A

15463399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: synonymous variant
orthologous variants: 141548757-C-T

15463486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: missense variant
orthologous variants: 141548670-T-C

15463528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141548628-T-G

http://identifiers.org/hco/1/GRCh38#15463550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141548600-C-A

15463550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141548600-C-T

15463617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141548561-G-C

15463635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141548543-G-A

15463635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141548543-G-T

http://identifiers.org/hco/1/GRCh38#15463639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141548539-C-A

15463639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141548539-C-T

15464223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141548247-G-A

15464223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141548247-G-C

15464238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 141548232-A-G

15464256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141548206-C-G

15464280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 141548183-G-A

15465362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141547166-T-A

15465451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141547101-C-T

15465514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141547059-A-G

15465548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141547025-A-T

15465554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141547019-G-A

15465669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546927-C-T

15465729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546877-T-C

15465794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546860-C-T

15465796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546858-G-A

15465797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546857-G-T

15465803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546851-G-A

15465803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546851-G-C

15465803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546851-G-T

http://identifiers.org/hco/1/GRCh38#15465804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141546850-A-C

15465804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546850-A-G

http://identifiers.org/hco/1/GRCh38#15465808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141546846-C-A

15465808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546846-C-T

15465838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546815-G-A

15465838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546815-G-T

http://identifiers.org/hco/1/GRCh38#15465886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141546743-C-A

15465886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546743-C-G

15465886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546743-C-T

15465887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546742-G-A

15465887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546742-G-C

15465887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546742-G-T

15465900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546724-G-T

http://identifiers.org/hco/1/GRCh38#15465915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141546711-C-A

15465915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141546711-C-G

15465936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141546496-C-G

15465936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141546496-C-T

15465945-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141546487-C-G

15465953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141546478-T-C

15465953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141546478-T-G

15465969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141546468-C-G

15465969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141546468-C-T

15466001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 141546434-A-G

15466001-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 141546434-A-T

15466118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141546317-G-A

http://identifiers.org/hco/1/GRCh38#15466153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141546281-C-A

15466157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546277-A-T

15466184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546256-G-A

15466185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546255-T-A

15466186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546254-G-A

15466477-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546251-A-T

15466484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546240-C-T

15466584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546142-G-C

15466584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546142-G-T

15466591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546135-T-G

15466801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546008-C-T

15466803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141546006-A-G

15467148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141545538-A-T

15467184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141545501-G-A

15467239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141545453-A-G

15467239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141545453-A-T

15467240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141545452-T-A

15467240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141545452-T-C

15467275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141545421-T-C

15467333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141545372-A-G

http://identifiers.org/hco/1/GRCh38#15467342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141545363-C-A

15467342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141545363-C-G

http://identifiers.org/hco/1/GRCh38#15467347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141545358-C-A

15467349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141545356-T-C

15467350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 141545355-C-T

15467458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141545254-G-A

15467458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 141545254-G-C

15467546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 141545166-C-G

15467546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 141545166-C-T

15469357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141544474-G-A

15469498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141544337-C-T

15469508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141544327-G-A

15469524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141544311-G-A

http://identifiers.org/hco/1/GRCh38#15469573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141544269-C-A

http://identifiers.org/hco/1/GRCh38#15469747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141543974-A-C

15469747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543974-A-G

15469878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543796-G-A

15469878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543796-G-C

15469878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543796-G-T

15469949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543745-T-C

15469986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543711-C-T

http://identifiers.org/hco/1/GRCh38#15470058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#141543647-C-A

15470058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543647-C-T

15470076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543630-A-G

15470093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543612-G-A

15470122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543593-G-A

15470139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543576-G-C

15470233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543493-G-A

15470233-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543493-G-C

15470234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543492-A-T

15470254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543434-A-T

15470301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543383-G-T

15470360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543334-C-T

15470437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543275-C-T

15470441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543271-C-T

15470462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543252-C-T

15470469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543245-T-C

15470515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543190-G-A

15470516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543189-G-A

15470553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141543156-C-T

15471963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141542391-C-T

15471964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141542390-T-C

15471970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 141542384-T-C

15472006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 141542348-A-T

15472037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141542321-C-T

15472038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141542320-T-A

15472041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141542317-G-A

15472053-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24609
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 141542305-A-T