http://identifiers.org/hco/2/GRCh38#189879587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53226810-C-A

http://identifiers.org/hco/2/GRCh38#189879659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53226730-C-A

189879659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 53226730-C-T

http://identifiers.org/hco/2/GRCh38#189879737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53226653-C-A

189879737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53226653-C-T

189879809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 53226597-T-C

189879913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53226493-C-T

http://identifiers.org/hco/2/GRCh38#189879916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53226489-C-A

189879916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53226489-C-T

189880111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53226128-G-A

189884001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224563-C-T

189884009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224555-C-T

189884259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224278-A-G

189884386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224170-T-C

189884422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224132-G-A

189884441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224113-G-T

189894680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222971-T-C

189894704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222919-A-G

189895020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222519-A-G

189895133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222329-T-C

189895212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222219-G-A

189895266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222153-T-C

http://identifiers.org/hco/2/GRCh38#189895282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53222137-A-C

189895282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222137-A-G

189895494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222013-G-A

189895531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221978-T-C

189896155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221644-A-G

189896293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221541-G-A

189896464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221399-C-T

http://identifiers.org/hco/2/GRCh38#189896580-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53221295-A-C

189896697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221164-A-G

189896810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221052-G-A

189897317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53220606-C-T

189899372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53211241-G-A

189899689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53210895-G-T

189899693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53210891-A-G

189902078-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53210150-T-G

http://identifiers.org/hco/2/GRCh38#189902222-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53209812-A-C

189902222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53209812-A-G

189902283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53209758-C-T

189902352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53209644-T-G

189902519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53209463-A-G

http://identifiers.org/hco/2/GRCh38#189902647-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53209350-A-C

http://identifiers.org/hco/2/GRCh38#189902741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53209263-C-A

189902754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53209250-A-G

189903275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53208850-A-G

189909899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53202286-G-A

http://identifiers.org/hco/2/GRCh38#189910071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53202104-C-A

189910390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53201765-A-G

189913066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53198053-T-C

http://identifiers.org/hco/2/GRCh38#189913190-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53197943-A-C

189913286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53197855-C-T

189913722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53197413-T-C

189913993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53197159-A-T

189914287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53196867-T-G

189914843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53196148-A-G

189915307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53195654-A-T

189915310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53195651-T-C

189915464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53195530-C-T

189915713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53195305-G-A

189932859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53187201-T-G

189932918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53187142-T-G

http://identifiers.org/hco/2/GRCh38#189932981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53187087-A-C

189933313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53186309-T-A

189933474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53186146-G-A

189933811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53185808-T-C

http://identifiers.org/hco/2/GRCh38#189933904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#53185724-A-C

189933908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53185720-A-G

http://identifiers.org/hco/2/GRCh38#189934279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#53185351-C-A

189934443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53185191-T-C

189934499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53185119-G-C

189934528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53185096-A-G

189934787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53184866-T-C

189934817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53184817-T-C

189935299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53184347-T-C

189935850-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53183874-T-G

189935958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53183747-T-A

189936027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53183665-A-T

189936337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53183440-A-G

189945706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53180752-T-C

189946231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53179569-G-A

http://identifiers.org/hco/2/GRCh38#189947743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53178131-A-C

189947860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53178026-A-T

189947871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53178015-T-C

189947886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53178000-C-G

189947956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53177926-C-G

189954316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53163687-T-C

http://identifiers.org/hco/2/GRCh38#189959268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53162780-C-A

189959631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53162474-G-C

189959632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53162473-T-A

189960197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53161872-C-T

189960216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53161853-T-G

http://identifiers.org/hco/2/GRCh38#189960380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53161722-A-C

189960628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53161481-G-T

189961128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53161219-G-A

189961203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53161145-C-T

189961205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53161143-G-A

189961283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53161055-G-A

189969205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53148526-T-C

189977486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53146177-A-G

190022728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53133682-A-G

190022777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53133639-T-C

190023164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53133335-A-G

190023343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53133219-G-A

190023359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53133207-G-A

190023578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53132972-G-T

190023631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53132927-C-T

190024515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53132210-A-G

190024883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53131712-T-C

190025042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53131477-A-G

190025091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53131429-C-G

190025289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53131259-A-T

190025336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53131214-C-T

190027015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53130172-A-G

190027345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53129732-A-G

190027417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53129664-T-G

190027769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53129317-G-A

190027769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53129317-G-C

190028031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53128944-A-G

190028309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53128486-A-G

190029417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53127608-G-A

190029723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53127393-A-G

190029787-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53127335-T-C

190029787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53127335-T-G

190029840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53127298-A-G

http://identifiers.org/hco/2/GRCh38#190029848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53127290-A-C

190030068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53127081-G-C

190030190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53126786-A-T

190030605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53126374-A-G

190030712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53126294-T-A

190030840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53126171-C-G

190030847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53126164-G-A

190030851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53126160-G-A

190030856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53126155-G-A

190031079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125935-C-T

190031106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125908-C-G

190031246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125817-G-T

190031352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125710-A-G

190031421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125647-G-A

190031695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125378-G-A

190031935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125135-G-A

190031935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125135-G-T

190032046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125028-A-T

190032629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53124393-C-T

190032691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53124335-C-T

190033094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53123728-C-T

190033404-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53123399-T-A

190033771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53123055-A-G

190033771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53123055-A-T

190033795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53123031-C-T

190033884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53122949-A-G

http://identifiers.org/hco/2/GRCh38#190034205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53122756-C-A

190034276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53122689-T-C

190034291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53122676-G-A

190035896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53119602-G-A

190035933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53119568-G-T

190035960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53119541-G-A

190035960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53119541-G-T

190036474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53118944-T-C

190036637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53118747-A-G

190036637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53118747-A-T

190036807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53118384-T-C

190037107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53117497-G-A

190037204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53117437-C-G

190037424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53117275-C-G

190047293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53114000-C-T

190047473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53113832-A-G

190047569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53113564-T-C

190047737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53113433-C-T

190049653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53111811-T-C

190049843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53111605-T-A

190050107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53111149-C-T

190050342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53110961-T-A

190050547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53110753-A-G

190051037-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53110386-C-G

190051104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53110357-G-A

190051136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53110319-A-G

190051180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53110262-C-G

190051219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53110230-A-G

190051254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53110201-G-C

190051325-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53110127-A-T

190051588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53109869-A-G

190052236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53109371-A-G

190052336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53109272-T-C

190052751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53108872-G-A

190053268-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53108420-T-G

190053576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53108129-T-A

190053707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53108003-G-A

190054021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53107624-T-G

190054218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53107433-A-G

190055507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53107415-C-G

http://identifiers.org/hco/2/GRCh38#190055628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53107325-C-A

190055871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53107076-A-G

190056122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53106864-T-C

190056534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53106491-A-G

190056549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53106475-G-T

190056577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53106447-T-G

http://identifiers.org/hco/2/GRCh38#190056579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53106445-C-A

190056678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53106347-G-T

190056749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53106292-A-G

190056943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53106107-A-G

190057511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53105535-G-C

190057511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 53105535-G-T

190057673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53105377-A-G

http://identifiers.org/hco/2/GRCh38#190057744-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53105312-A-C

http://identifiers.org/hco/2/GRCh38#190057834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53105205-A-C

190057916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53105121-A-G

190058088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53104986-A-G

190058119-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53104948-T-A

190058243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53104675-T-G

http://identifiers.org/hco/2/GRCh38#190060477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53103001-C-A

190060537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53102947-G-T

http://identifiers.org/hco/2/GRCh38#190060805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53102672-A-C

190061541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101966-G-C

190062010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101506-T-C

190062027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101489-A-G

190062176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101346-G-C

190062176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101346-G-T

http://identifiers.org/hco/2/GRCh38#190062721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53100806-A-C

190063117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53100414-T-A

190063358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53100187-T-C

190064022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53099534-G-A

190064216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53099336-C-T

190064288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53099265-A-T

190064733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098854-G-A

190064747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098840-T-A

190065033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098728-T-A

190065047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098714-C-T

190065050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098711-A-G

190065143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098584-G-A

190065143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098584-G-T

190065161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098571-C-T

190065243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098510-A-G

190065503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098254-T-G

190065678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098021-A-G

190065849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53097846-T-C

190065901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53097794-C-G

190065941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53097769-T-C

190066155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53097587-C-T

190066431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53097330-G-A

190066443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53097318-A-G

190066463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53097298-T-G

190066502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53097263-G-A

190066510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53097255-C-T

190066619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53097146-A-G

190066867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53096925-A-T

190066902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53096889-C-T

190067354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53095824-G-A

190067376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53095804-A-G

190067454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53095745-G-A

190067454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53095745-G-T

190069367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53093861-A-G

190070111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53093528-A-T

190071780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53091984-G-A

http://identifiers.org/hco/2/GRCh38#190071851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53091912-C-A

190071851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53091912-C-T

190072562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53091588-G-T

190072598-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53091565-T-G

190072805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53091368-C-T

190074217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53086464-A-G

190074538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53086129-C-G

http://identifiers.org/hco/2/GRCh38#190074643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53086041-C-A

190074665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53086019-A-G

190079927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53077632-T-G

190080328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53077232-A-G

190080332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53077228-G-C

190080492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53077066-G-T

190080755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53076815-T-G

190080847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53076719-A-G

190080979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53076598-G-A

190082823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53076082-C-T

190082845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53076064-T-A

190084906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53074535-G-A

190084993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53074447-T-C

190085038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53074396-C-T

190085048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53074386-G-T

190086792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53074236-G-A

190087010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53074058-G-A

190087014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53074054-T-C

190087381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53073435-G-T

190087570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53073237-T-G

190087827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53072980-T-C

190087947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53072854-G-A

190088034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53072774-T-G

190088067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53072741-G-A

190088067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53072741-G-T

http://identifiers.org/hco/2/GRCh38#190088088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53072720-C-A

http://identifiers.org/hco/2/GRCh38#190088223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53072630-C-A

190088350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53072504-A-T

190088413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53072437-C-T

190089306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53071735-A-T

190089386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53071715-G-A

http://identifiers.org/hco/2/GRCh38#190089472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53071631-A-C

http://identifiers.org/hco/2/GRCh38#190089683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53064024-C-A

190089683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53064024-C-T

190089846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53063870-G-A

190090037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53063687-G-A

http://identifiers.org/hco/2/GRCh38#190090779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53062377-C-A

190090824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53062333-T-C

190091249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53061950-A-G

190091304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53061899-C-T

190091527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53061677-T-G

190091588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53061614-G-A

190091628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53061575-G-A

190091815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53061210-A-G

190092905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53060106-G-A

http://identifiers.org/hco/2/GRCh38#190093504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53059845-A-C

190093778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53059571-T-C

http://identifiers.org/hco/2/GRCh38#190093806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53059543-A-C

190094054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53059286-G-C

190094073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53059268-A-G

190094556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53058175-T-A

190094884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53057852-T-A

190095490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53057593-T-C

190095560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53057523-G-C

190099974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53055692-A-G

190100120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53055549-G-A

190100120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53055549-G-T

190100259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53055418-A-G

http://identifiers.org/hco/2/GRCh38#190100306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53055372-A-C

190100464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53055291-T-C

190100509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53055249-A-G

190100604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53055165-G-A

190100657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53055112-A-T

190106614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53054425-G-A

190106986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53054079-G-C

http://identifiers.org/hco/2/GRCh38#190107017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53054050-A-C

190107017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53054050-A-G

190107268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53053798-A-G

190107520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53053547-T-C

190107651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53053416-G-C

190108500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53052811-A-G

190108526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53052803-T-G

190108745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53052661-G-A

190108868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53052472-C-T

190108877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53052464-A-T

190108942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53052343-G-A

190108951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53052334-C-T

190108984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53052300-T-C

http://identifiers.org/hco/2/GRCh38#190109132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53052167-A-C

190109186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53052120-T-C

190109512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53051946-G-C

190109521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53051934-G-A

190109530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53051925-C-T

http://identifiers.org/hco/2/GRCh38#190109564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53051889-C-A

190109564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53051889-C-T

190109634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53051819-G-A

190109710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53051792-G-C

190109763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53051750-T-C

190109813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53051701-C-T

190110034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53051492-T-C

190110391-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53050465-C-G

http://identifiers.org/hco/2/GRCh38#190110545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53050336-C-A

190110545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53050336-C-T

190110578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53050303-T-A

190110578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53050303-T-G

http://identifiers.org/hco/2/GRCh38#190111204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53049692-C-A

190111586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53049318-G-A

190112329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53048465-A-G

190113071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047938-T-G

190113122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047858-C-G

190113155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047825-T-C

190113158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047822-A-G

190113228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047749-T-C

190113290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047697-G-A

190113290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047697-G-T

190113329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047648-C-T

http://identifiers.org/hco/2/GRCh38#190113524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53047410-C-A

http://identifiers.org/hco/2/GRCh38#190113623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53047310-C-A

190137378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53011580-A-G

190137567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53011406-G-T

190138327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53010715-A-G

190142500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53010082-G-T

190162541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53006952-T-C

190162736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53006752-G-A

190169473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53002683-A-T

190169653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53002509-A-G

http://identifiers.org/hco/2/GRCh38#190169906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53002253-C-A

190169941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53002219-A-G

190170000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53002188-A-G

http://identifiers.org/hco/2/GRCh38#190170098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#53002097-C-A

190170099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53002096-A-G

http://identifiers.org/hco/2/GRCh38#190170529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52998316-C-A

190170560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52998289-C-T

190170596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52998256-C-T

190170673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52998187-C-T

190170755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52998100-T-C

http://identifiers.org/hco/2/GRCh38#190170969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52997871-C-A

190170969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52997871-C-G

190171288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52997551-G-A

http://identifiers.org/hco/2/GRCh38#190171303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52997537-A-C

190171343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52997497-T-C

190171417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52997409-T-G

190171855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52996729-G-A

190172227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52996390-C-T

190172362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52996295-C-G

190172429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52996230-A-G

190172444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52996212-T-C

190173293-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52995608-A-T

190174728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52995271-A-G

http://identifiers.org/hco/2/GRCh38#190178232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52994518-C-A

190178284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52994464-A-G

190178315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52994439-C-T

190178409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52994384-G-A

190178502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52994296-C-T

190178516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52994282-C-T

190178524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52994275-T-C

190178606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52994242-T-C

190178614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52994234-C-T

190178878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52993616-C-T

190179045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52993497-C-T

190179046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52993496-A-G

190179647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52993247-A-G

190179663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52993231-C-T

http://identifiers.org/hco/2/GRCh38#190179954-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#52992752-A-C

190180072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52992648-A-T

190180268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52992462-A-G

190180287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52992445-C-G

190180287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52992445-C-T

190180329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52992404-C-G

190180329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52992404-C-T

190180339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52992394-A-T

190180386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52992383-A-G

http://identifiers.org/hco/2/GRCh38#190180423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52992346-C-A

190180423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52992346-C-G

190180423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52992346-C-T

190180430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52992339-C-T

190180447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52992319-G-A

190180461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52992306-A-T

http://identifiers.org/hco/2/GRCh38#190180562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#52992247-C-A

190180562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52992247-C-T

190180568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992241-G-A

190180568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992241-G-T

190180626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992195-C-T

http://identifiers.org/hco/2/GRCh38#190180635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52992186-C-A

190180635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992186-C-G

190180635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992186-C-T

190180642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992179-G-A

190180642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992179-G-T

http://identifiers.org/hco/2/GRCh38#190180679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52992146-C-A

190180699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992126-T-C

http://identifiers.org/hco/2/GRCh38#190180738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#52992100-C-A

190180738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52992100-C-T

http://identifiers.org/hco/2/GRCh38#190180751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#52992088-C-A

190180751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52992088-C-G

190180751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52992088-C-T

http://identifiers.org/hco/2/GRCh38#190180765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#52992078-C-A

190180765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52992078-C-T

190180792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992051-G-A

190180792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992051-G-C

190180792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992051-G-T

190180802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992041-G-A

190180841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992000-G-A

190180841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52992000-G-T

190180907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52991961-G-A

190180913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52991955-G-A

190180913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52991955-G-T

http://identifiers.org/hco/2/GRCh38#190180914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52991954-C-A

190180914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52991954-C-T

http://identifiers.org/hco/2/GRCh38#190180923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52991949-C-A

190180923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52991949-C-T

http://identifiers.org/hco/2/GRCh38#190180950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52991928-C-A

190180980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52991890-G-A

190181010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52991859-A-G

http://identifiers.org/hco/2/GRCh38#190181048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52991832-C-A

190181050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52991830-C-T

http://identifiers.org/hco/2/GRCh38#190181051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52991829-C-A

190181051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52991829-C-G

190181051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52991829-C-T

http://identifiers.org/hco/2/GRCh38#190181079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#52991803-A-C

190181079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52991803-A-G

190181082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 52991800-G-T

190181132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52991749-G-A

http://identifiers.org/hco/2/GRCh38#190181219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52991690-A-C

190181434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52991488-G-A

190181434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52991488-G-T

http://identifiers.org/hco/2/GRCh38#190181500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52991430-C-A

190181500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52991430-C-T

http://identifiers.org/hco/2/GRCh38#190181786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52991171-A-C

190181914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52991076-A-G

190181960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52991044-T-C

190182159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52990844-G-A

190182208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52990802-C-T

190182226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52990784-G-A

190182853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52990361-T-C

190183110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52990138-G-A

190183501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52989811-C-T

190183660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52989464-T-A

190183713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52989415-G-C

190183768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52989360-A-G

190183933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52989226-T-A

190184937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52989102-T-C

190185087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52988972-T-C

190185100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52988959-A-G

190185289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52988768-G-A

190185603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52988451-G-C

190185718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52988316-T-A

190186482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52987746-G-A

190186876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52987327-A-G

190187206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52987002-A-G

190187354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52986891-T-C

190187402-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 52986844-G-T

190195249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52974017-A-G

190195507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52973738-A-G

190195547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52973691-T-C

190195573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52973678-C-T

http://identifiers.org/hco/2/GRCh38#190195873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52973330-C-A

190196366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52972461-T-C

190196446-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52972369-T-A

190196490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52972317-C-T

190196516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52972288-C-T

http://identifiers.org/hco/2/GRCh38#190197883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52966809-C-A

190197883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52966809-C-T

190197946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52966762-A-G

190198101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52966605-T-C

190198122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52966584-G-A

190198196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52966496-G-C

190199522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52965027-T-C

190199570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52964983-A-G

http://identifiers.org/hco/2/GRCh38#190199586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52964967-C-A

190199586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52964967-C-G

190199586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52964967-C-T

190199626-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 52964937-T-G

190199699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 52964889-A-G

http://identifiers.org/hco/2/GRCh38#190199771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52964820-C-A

190199771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 52964820-C-T

190199930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 52964655-A-G

http://identifiers.org/hco/2/GRCh38#190200325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52964273-C-A

190200325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52964273-C-T

http://identifiers.org/hco/2/GRCh38#190200328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52964270-C-A

190200328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52964270-C-T

http://identifiers.org/hco/2/GRCh38#190200604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52963950-C-A

190200604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52963950-C-T

190200608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52963946-A-G

http://identifiers.org/hco/2/GRCh38#190200954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52963585-C-A

190200992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52963560-G-A

190200992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52963560-G-T

190201403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52963229-T-C

190201832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52962820-T-C

190202076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52962627-T-G

190202139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52962585-G-C

190202139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52962585-G-T

http://identifiers.org/hco/2/GRCh38#190202167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#52962566-A-C

190202167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52962566-A-G

190202666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52962202-A-T

190202685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52962183-G-C

190202733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52962140-A-G

190202844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52962067-A-G

190202891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52962026-G-T

190202899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52962018-T-C

190202917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52962000-T-C

190203061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52961866-A-G

190203099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52961832-C-T

190203114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52961815-G-A

190203137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28191
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 52961801-G-T