31867932-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74507806-T-G

http://identifiers.org/hco/2/GRCh38#31868171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74508003-C-A

31868171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74508003-C-G

31868283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74508113-G-A

http://identifiers.org/hco/2/GRCh38#31868300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74508130-A-C

31868406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74508234-T-C

http://identifiers.org/hco/2/GRCh38#31868538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74508365-C-A

31868538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74508365-C-G

31868538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74508365-C-T

31869766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74509172-G-C

31869766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74509172-G-T

http://identifiers.org/hco/2/GRCh38#31869770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74509176-C-A

31869770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74509176-C-T

http://identifiers.org/hco/2/GRCh38#31869803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74509218-C-A

31869826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74509235-A-G

31869826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74509235-A-T

31870008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74509386-A-G

31870181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74509536-T-C

31870204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74509554-T-C

31870206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74509556-T-C

31870283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74509620-G-A

31870930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74509876-C-G

31871413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74510528-G-A

31871547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74510631-T-C

31872286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74511131-G-C

http://identifiers.org/hco/2/GRCh38#31873087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74511910-C-A

31873138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74511960-G-A

31873138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74511960-G-C

31873218-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74512031-A-T

31874165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74512931-T-C

31874189-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74512972-T-A

31874201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74512984-T-C

31874294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74513117-T-C

31875400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74514759-T-C

http://identifiers.org/hco/2/GRCh38#31875589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74514912-C-A

31878372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74517138-C-T

31878626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74517417-G-A

31878688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74517479-G-C

31878698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74517510-G-A

31878698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74517510-G-C

31879004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74518018-T-C

31879023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74518037-T-A

31879209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74518348-G-A

31879297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74518400-T-C

31881522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74522841-G-A

31881522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74522841-G-C

31881522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74522841-G-T

http://identifiers.org/hco/2/GRCh38#31881544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74522872-C-A

31881544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74522872-C-G

http://identifiers.org/hco/2/GRCh38#31881545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74522873-C-A

31881550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74522878-G-A

31883005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74523665-A-T

31883095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74523750-G-A

31883204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74523857-G-A

31883648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74524289-T-A

31884012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74524602-C-G

31884012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74524602-C-T

31884315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74524855-A-T

31884561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525228-T-A

31884561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525228-T-G

31884685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525343-C-G

31884752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525391-C-T

31884960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525555-A-G

31884961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525556-T-A

31884964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525559-T-C

31885430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74525982-T-C

http://identifiers.org/hco/2/GRCh38#31885498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74526051-A-C

31885537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74526087-T-G

http://identifiers.org/hco/2/GRCh38#31885907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74526417-C-A

31885936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74526450-C-T

31886352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74526814-G-A

31886413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74526879-T-C

31886546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74527014-G-A

31886793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74527243-A-G

31886882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74527329-T-C

31886934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74527379-G-C

31887317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74527761-G-A

31887455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74527897-A-G

31887581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74528016-A-T

31887673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74528109-G-C

31888591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74528850-G-T

31890180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74530837-C-T

31890438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74531051-C-G

31890603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74531205-C-T

31890748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74531283-C-T

31890756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74531291-G-T

31890814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74531345-G-A

31890850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74531362-G-A

31891335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74531812-C-T

31891404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74531880-C-G

31891500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74531944-T-C

31892255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74532702-A-G

31892311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74532752-G-A

31892562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74532966-T-C

31892632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74533036-G-T

http://identifiers.org/hco/2/GRCh38#31892638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74533042-C-A

31892638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74533042-C-G

31892638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74533042-C-T

31892792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74533166-C-T

http://identifiers.org/hco/2/GRCh38#31893134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74533452-A-C

31893134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74533452-A-G

31893221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74533546-T-C

31893221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74533546-T-G

31893292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74533617-A-G

31893292-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74533617-A-T

31893306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74533631-T-C

31893461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74533801-G-A

31893461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74533801-G-T

31893803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74534136-C-T

31893854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74534183-T-C

31915279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74546410-T-A

31915401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74546528-G-A

http://identifiers.org/hco/2/GRCh38#31915594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74546616-C-A

31915604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74546625-G-A

31915739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74546681-G-A

31917073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74547928-G-A

31917315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74548289-A-T

31917399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74548369-T-C

31917399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74548369-T-G

31917542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74548517-C-T

31917861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74548833-T-C

31918096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74549070-A-G

31918096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74549070-A-T

31918131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74549089-T-C

31918277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74549175-G-A

31918638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74549504-C-T

31920409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74551618-T-A

31920409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74551618-T-C

31920730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74551904-A-T

31920737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74551911-T-C

31920737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74551911-T-G

31921098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74552283-T-C

31921498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74552801-C-T

31921833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74552991-A-G

31923433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74554180-T-A

31923433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74554180-T-C

31923563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74554295-G-A

31923563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74554295-G-T

http://identifiers.org/hco/2/GRCh38#31923849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74554899-C-A

31923849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74554899-C-G

31923849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74554899-C-T

31923880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74554931-G-A

31923880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74554931-G-T

31924258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74555278-G-C

31924350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74555360-G-T

31924932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74555901-G-A

31925349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556087-G-A

http://identifiers.org/hco/2/GRCh38#31925400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74556136-C-A

31925400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556136-C-T

31925418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556156-G-A

31925425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556160-G-A

31925453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556179-G-A

31925453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556179-G-C

31925455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556181-G-A

31925455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556181-G-C

31925459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556185-G-A

31925459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556185-G-C

31925459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556185-G-T

31925698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74556964-T-C

31925780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557038-C-G

http://identifiers.org/hco/2/GRCh38#31925806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74557056-A-C

31925853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557099-G-T

31926001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557247-T-C

31926011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74557257-A-G

31928804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74560993-C-T

31930515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74561783-T-A

31930562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74561827-T-C

http://identifiers.org/hco/2/GRCh38#31931815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74562044-A-C

31931815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74562044-A-G

http://identifiers.org/hco/2/GRCh38#31932120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74562276-C-A

31932120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74562276-C-T

31932275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74562426-T-C

http://identifiers.org/hco/2/GRCh38#31932283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74562434-C-A

31943420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74565537-G-T

31943447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74565563-G-A

31943447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74565563-G-T

31943468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74565584-T-G

31943479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74565595-A-G

31943497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74565613-A-G

31943498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74565614-T-C

31943514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74565630-G-A

31943514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74565630-G-T

31943517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74565633-G-A

31943517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74565633-G-T

31943539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74565659-T-C

31943709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74565791-T-C

31943959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74566340-T-C

31943997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74566377-C-T

31944032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74566420-T-C

31944059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74566447-T-C

http://identifiers.org/hco/2/GRCh38#31944075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74566462-C-A

31944115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74566492-C-T

31944558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74567234-T-G

31944563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74567238-C-T

31944586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74567263-G-A

31955249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74568151-T-C

31960254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74570935-C-T

31960990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74573865-T-C

31961889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74575755-T-C

31962332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74578070-G-A

31962423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74578165-G-C

31987940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74582379-C-T

31987945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74582388-T-C

http://identifiers.org/hco/2/GRCh38#31987963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74582408-C-A

31987986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74582431-T-C

31997709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74590461-T-C

http://identifiers.org/hco/2/GRCh38#31997725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74590475-A-C

31997748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74590498-T-A

31997764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74590513-G-A

31997922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74590620-C-T

31997975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74590711-G-A

31998555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74591383-C-T

31998572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74591401-G-A

31998967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74591597-T-C

32006021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74598006-T-C

32006100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74598085-G-C

http://identifiers.org/hco/2/GRCh38#32006117-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74598101-A-C

http://identifiers.org/hco/2/GRCh38#32006592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74598525-A-C

32006592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74598525-A-G

32006758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74598615-A-G

32006758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74598615-A-T

http://identifiers.org/hco/2/GRCh38#32007255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74599019-A-C

32007481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74599238-T-C

32007776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74599517-A-T

32008060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74599885-T-C

32008060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74599885-T-G

32008456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74600240-C-T

32008563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74600335-G-A

32009075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74600911-T-C

32009409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74601231-C-T

32009550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74601382-G-C

32009811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74601494-A-G

http://identifiers.org/hco/2/GRCh38#32010040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74601587-C-A

32010040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74601587-C-G

32010239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74601739-G-A

32010239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74601739-G-C

32010239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74601739-G-T

http://identifiers.org/hco/2/GRCh38#32010384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74601875-C-A

32010384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74601875-C-G

32010384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74601875-C-T

32010426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74601908-A-G

32010426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74601908-A-T

32010430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74601912-G-A

32010430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74601912-G-C

32010430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74601912-G-T

http://identifiers.org/hco/2/GRCh38#32010516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74601993-C-A

32010559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74602040-G-A

32010559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74602040-G-T

32010582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74602058-T-A

32010847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74602301-A-G

32011105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74602582-C-T

32011182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74602669-T-C

http://identifiers.org/hco/2/GRCh38#32011249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#74602747-C-A

32011249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74602747-C-G

32011249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74602747-C-T

32011252-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74602750-G-T

32011260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74602758-T-C

32011264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74602762-T-A

32011279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74602777-G-A

32011279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74602777-G-T

http://identifiers.org/hco/2/GRCh38#32011290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#74602788-C-A

32011290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74602788-C-T

32012038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74603187-G-A

32012038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74603187-G-C

32012038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74603187-G-T

http://identifiers.org/hco/2/GRCh38#32013489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74604398-C-A

32022807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74605634-C-T

32023049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74605820-G-T

32023186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74605873-G-T

32023280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74605943-C-G

32023280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74605943-C-T

32023338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74606000-T-G

32023815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74606414-C-T

32023965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74606538-A-G

32024088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74606650-A-G

32024311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74606872-T-A

32024340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74606894-A-T

32024356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74606912-T-C

32024362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74606918-T-C

32024401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74606957-G-A

32024401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74606957-G-C

32024405-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74606961-T-A

32028518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74611567-T-A

http://identifiers.org/hco/2/GRCh38#32029024-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74614080-A-C

32029064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74614139-G-C

32029144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74614244-C-T

32029248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74614337-G-A

32029268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74614357-T-C

http://identifiers.org/hco/2/GRCh38#32029514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74614643-A-C

http://identifiers.org/hco/2/GRCh38#32029516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74614645-A-C

http://identifiers.org/hco/2/GRCh38#32029524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74614654-A-C

32029524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74614654-A-G

32029551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74614680-T-C

32029761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74614881-A-G

http://identifiers.org/hco/2/GRCh38#32029767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74614890-A-C

32029810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74614934-G-A

32029820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74614943-C-G

32039263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74622881-G-C

http://identifiers.org/hco/2/GRCh38#32039367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74622984-C-A

32039367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74622984-C-G

32039367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74622984-C-T

http://identifiers.org/hco/2/GRCh38#32039482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74623101-C-A

32039482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 74623101-C-G

32039612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74623221-G-A

32039612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74623221-G-C

32039612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74623221-G-T

http://identifiers.org/hco/2/GRCh38#32039708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#74623315-A-C

32039708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24590
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74623315-A-G