76439063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17358246-T-C

76439105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17358205-G-A

76439157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17358149-A-G

76439201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17358110-A-G

76439733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17357390-T-G

76439898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17357292-G-A

76439962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17357231-T-G

76440293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17357018-A-G

76441625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-A

76441625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-T

76441636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-A

76458729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17334433-G-A

http://identifiers.org/hco/9/GRCh38#76458816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17334344-A-C

76458819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17334341-T-C

http://identifiers.org/hco/9/GRCh38#76458957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17334220-C-A

76459032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17334141-T-A

76459032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17334141-T-C

76459048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17334125-G-A

76459048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17334125-G-T

http://identifiers.org/hco/9/GRCh38#76459055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#17334118-C-A

http://identifiers.org/hco/9/GRCh38#76459069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#17334105-C-A

76459069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17334105-C-T

76459071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17334103-G-A

76459126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17334077-C-T

76459138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17334061-G-T

76459218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17333998-G-A

76459218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17333998-G-C

76459218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17333998-G-T

76459264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17333957-T-C

76459264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17333957-T-G

76459266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17333955-G-T

76459267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17333954-G-A

76459267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17333954-G-T

76459278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17333943-A-G

76459279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17333942-G-T

http://identifiers.org/hco/9/GRCh38#76459310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17333914-C-A

76459359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333888-G-A

76459370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333877-T-G

76459414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333851-G-A

76459452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333805-G-A

76459452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333805-G-T

76459454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333803-G-C

76459454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333803-G-T

76459509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333742-T-A

76459554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333702-G-A

76459562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333694-C-T

76459765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333506-A-G

76459859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333442-C-T

76459938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333364-C-T

http://identifiers.org/hco/9/GRCh38#76459945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17333357-C-A

76459963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333332-T-C

76460218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333065-A-G

76460275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17333009-T-C

76460457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17332834-T-G

76460568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 17332717-T-A

76462160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 17332325-A-T

76462190-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17332295-T-G

76462311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17332165-A-G

76463040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17330750-G-A

76463040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17330750-G-C

76463040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17330750-G-T

76463259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17330547-T-C

76463323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17330492-G-T

76463336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17330478-T-G

76463509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17330259-C-T

76463624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17330145-A-G

76463664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17330116-G-A

76464085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17329848-A-G

76464148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17329785-G-A

76464148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17329785-G-T

76464225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17329609-T-G

76464324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17329521-C-T

76464342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17329503-G-A

76464344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17329501-G-A

76471706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17325465-T-C

http://identifiers.org/hco/9/GRCh38#76472516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#17324048-C-A

76472541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17324023-T-G

76472616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17323974-G-A

76472710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17323896-A-G

76473108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17323837-C-T

76473400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17323564-G-A

76475529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17320225-G-A

76475642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17320043-T-C

76476699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17319396-T-C

76480544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17316905-C-T

http://identifiers.org/hco/9/GRCh38#76487421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17316646-A-C

76499914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17311857-G-A

76499970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17311804-G-A

76499970-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17311804-G-C

76499970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17311804-G-T

76500376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17311287-G-A

76500395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17311268-A-T

76500695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17310881-C-G

76500708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17310871-T-C

76500858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17310684-A-G

http://identifiers.org/hco/9/GRCh38#76500996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17310540-C-A

76501029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17310504-C-T

http://identifiers.org/hco/9/GRCh38#76501088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17310439-C-A

76501088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17310439-C-T

76501436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17308818-A-G

76501499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17308762-A-G

76501664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17308624-T-C

76501664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17308624-T-G

76501666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17308622-A-G

http://identifiers.org/hco/9/GRCh38#76501746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17308543-C-A

76501965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17308304-C-T

76502260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17307860-G-A

76502260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17307860-G-T

76502422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17307681-C-T

76503011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 17307092-G-A

76503012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17307091-A-G

http://identifiers.org/hco/9/GRCh38#76503056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17307047-C-A

76503056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17307047-C-T

76503112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17306991-C-T

76503119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17306984-G-A

76503119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17306984-G-C

76503119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17306984-G-T

76503387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17306716-C-T

76503493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17306610-C-T

76503693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17306413-A-G

http://identifiers.org/hco/9/GRCh38#76503729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17306377-C-A

76503729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17306377-C-G

76503729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17306377-C-T

76503847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17306279-T-C

76503847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17306279-T-G

http://identifiers.org/hco/9/GRCh38#76503867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17306263-C-A

76503870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17306260-G-A

76504026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17306107-T-A

76504026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17306107-T-C

76504035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17306098-A-T

76504258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17305882-T-C

76504258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17305882-T-G

76504277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17305863-G-T

76504383-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17305678-T-A

76504494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17305577-T-C

76504503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17305568-A-G

76504503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17305568-A-T

76504597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17305483-G-C

76504597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17305483-G-T

http://identifiers.org/hco/9/GRCh38#76504709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17305387-C-A

76504970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17305210-T-C

76505114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17305065-T-C

http://identifiers.org/hco/9/GRCh38#76505302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17304895-C-A

http://identifiers.org/hco/9/GRCh38#76505558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17304673-C-A

76505805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17304381-T-C

76505901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17304271-A-G

76505915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17304258-A-G

76506144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17304031-C-T

76506708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17303759-A-T

76506724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17303743-T-C

76506724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17303743-T-G

76510498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17301442-A-G

76510553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17301327-T-C

76510553-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17301327-T-G

http://identifiers.org/hco/9/GRCh38#76510677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17300642-A-C

76510715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17300609-A-G

76511007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17300322-T-G

76516433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17290472-A-G

76516770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: non coding transcript exon variant
orthologous variants: 17290173-G-A

76516930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17289463-A-G

76517078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17289327-C-G

76517078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17289327-C-T

76517163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17289262-T-G

76519050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17286962-T-G

76519105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17287017-A-G

76519219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17287115-G-C

76519243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17287139-G-A

76519281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17287157-G-A

76519343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17287206-A-G

76519372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17287233-G-A

76519378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17287238-T-G

76519573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17287443-G-A

76550455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17267702-C-T

76550461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17267696-A-G

76550541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17267662-G-T

76550597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17267630-G-A

76550853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17267407-T-G

76550938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17267317-T-C

76551268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17267002-A-T

76551299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17266971-T-G

76551398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17266873-A-G

76551523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17266698-C-T

76551830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17266201-G-A

76551830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17266201-G-T

76551854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17266177-A-G

76551954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17264933-C-T

76552327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17264355-C-T

76552582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17264103-T-C

76552640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17264045-A-G

76552718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17263744-G-A

http://identifiers.org/hco/9/GRCh38#76553152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17263355-C-A

76553193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17263315-C-G

76553193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17263315-C-T

http://identifiers.org/hco/9/GRCh38#76553208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17263300-C-A

76553578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17262938-A-G

76553694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17262831-T-C

76559787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17249798-A-G

76559980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17249672-A-T

76560042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17249624-G-T

76560100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17249577-C-T

76560132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17249544-G-C

76560194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17249478-G-A

76560248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17249421-C-T

76560346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17249151-C-T

76560445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17249056-G-A

76560608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17248863-G-A

76560742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17248730-G-T

76560892-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17248589-C-G

76561123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17248398-C-G

76561259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17248272-T-C

76561477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17248083-A-G

76561529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17248025-A-T

76561700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17247830-T-C

76561916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17247591-C-G

76562116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17247404-T-C

76562357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17247250-C-T

76576422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17241354-G-A

76576429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17241347-A-T

76576453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17241328-G-A

76576833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17241056-A-G

76576976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17240916-G-C

76576976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17240916-G-T

76582481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17237991-C-T

76582821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17237595-G-A

76582831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17237585-C-T

76582860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17237569-A-G

http://identifiers.org/hco/9/GRCh38#76583268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17237264-A-C

76583357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17237173-C-G

76583357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17237173-C-T

76583363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17237167-C-G

76583368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17237162-A-G

76583368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17237162-A-T

76583396-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17237135-T-G

76583435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17237100-G-A

76586418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17235979-G-A

76586442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17235955-G-A

76586798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17235143-T-G

76586841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17235098-G-C

76586918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17235061-G-T

76586998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17235002-G-C

76587120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17234897-T-A

76587152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17234875-G-A

76587193-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17234834-T-A

76587370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17234657-A-G

76587581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17234569-G-A

76587713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17234431-G-A

76587714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17234430-G-T

76587795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17234337-G-A

76589414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17233624-C-T

http://identifiers.org/hco/9/GRCh38#76589435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17233603-A-C

76589435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17233603-A-G

76589497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17233548-T-C

76589512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17233534-T-A

76589546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17233503-T-C

76589753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17233294-A-G

76589788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17233259-T-G

76589912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17233140-C-T

76589970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17233075-G-A

76590046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17233011-C-T

76590085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17232971-T-C

76590099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17232945-A-G

76590148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17232891-G-A

76590238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17232804-A-G

76590255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17232787-G-A

76590255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17232787-G-C

76590256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17232786-T-A

76591256-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17232607-T-A

http://identifiers.org/hco/9/GRCh38#76591660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17232288-A-C

76591758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17232047-G-A

76591766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17232038-G-A

76591847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17231923-C-T

76591867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17231903-T-C

76591899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17231874-C-T

76591951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17231824-C-G

76591951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17231824-C-T

76591984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17231793-T-A

76591992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17231785-T-C

76592059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17231718-G-A

76592094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17231686-T-C

76592199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17231581-G-A

76592299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17231488-A-G

76592326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17231454-T-C

76592356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17231423-G-A

76592549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17230870-G-T

76592713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17230723-C-T

76592819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17229176-C-T

76592840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17229157-C-T

76598038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17226120-T-G

76598856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17225695-G-A

76599025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17225571-A-G

http://identifiers.org/hco/9/GRCh38#76599231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17225435-C-A

76599277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17225379-T-C

76600259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17222456-C-T

76600286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17222429-A-G

76600300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17222416-T-C

76600432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17222294-C-T

76600434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17222286-A-G

76600492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17222225-G-A

76600508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17222209-C-T

76600527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17222190-C-T

http://identifiers.org/hco/9/GRCh38#76603405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17218440-C-A

76603502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17218350-C-G

76603866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17217993-A-G

76603984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17217888-A-T

76604196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17217675-C-T

http://identifiers.org/hco/9/GRCh38#76604303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17217471-A-C

76607131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17213944-T-C

76607178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17213896-C-T

76607212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17213866-A-G

76607287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17213801-A-G

76607310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17213779-C-T

http://identifiers.org/hco/9/GRCh38#76607311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17213778-A-C

http://identifiers.org/hco/9/GRCh38#76607345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17213746-A-C

76607389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17213702-A-G

76607400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17213690-T-C

http://identifiers.org/hco/9/GRCh38#76608064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17205664-A-C

76608165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17205580-T-C

76608212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17205531-T-C

76608265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17205465-T-C

76608861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17205041-G-A

76609001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17204905-G-A

76609173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17204748-A-T

76609728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17204298-G-C

76609928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17204134-G-A

76611751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17200916-A-G

76611925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17200736-A-G

76611958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17200702-G-T

http://identifiers.org/hco/9/GRCh38#76611963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17200697-A-C

http://identifiers.org/hco/9/GRCh38#76612333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17200361-C-A

76612333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17200361-C-G

76614817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17197497-C-T

76614909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17197413-A-G

76614980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17197323-T-C

76615214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17196985-T-A

76615214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17196985-T-C

76615222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17196978-A-G

76615274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17196919-C-T

76615375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17196821-T-C

http://identifiers.org/hco/9/GRCh38#76615522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17196690-C-A

76616182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17196436-C-G

76616182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17196436-C-T

76616561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17196216-T-C

76616727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17196037-C-G

76616727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17196037-C-T

76617005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17195812-T-A

76617523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17195303-A-G

76617562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17195268-T-C

76617756-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17195078-C-G

76617765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17195070-G-A

76618043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17194820-G-A

76618275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17194679-C-T

76618302-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17194656-T-A

76618366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17194613-T-C

76618431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17194555-A-G

76619080-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17193982-A-T

http://identifiers.org/hco/9/GRCh38#76619243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17193833-A-C

76619243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17193833-A-G

76619282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17193793-G-A

76619282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17193793-G-C

76619282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17193793-G-T

76619330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17193745-G-A

76619330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17193745-G-C

76619330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17193745-G-T

76619371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17193704-T-C

76619371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17193704-T-G

http://identifiers.org/hco/9/GRCh38#76619487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17193570-C-A

76619487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17193570-C-G

76619487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17193570-C-T

76619531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17193521-G-A

76619537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17193515-G-A

76619537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17193515-G-T

http://identifiers.org/hco/9/GRCh38#76619563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17193485-A-C

76619935-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17193085-T-G

76619938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17193082-A-G

76620105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17192915-A-G

76620110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17192910-T-C

76620471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17192625-A-G

76620742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17192377-C-T

76620856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17192268-C-T

http://identifiers.org/hco/9/GRCh38#76621182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17191955-C-A

76621200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17191937-A-G

76621219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17191926-C-T

76621411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17191531-T-G

76621442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17191500-G-A

76621492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17191466-T-C

76621492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17191466-T-G

76622932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17191357-T-C

76623885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17190471-G-T

76624147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17190001-C-T

76624240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17189907-C-T

http://identifiers.org/hco/9/GRCh38#76624380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17189764-C-A

76624380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17189764-C-T

76624421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17189724-T-C

76624421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17189724-T-G

76624422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17189723-G-A

76624422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17189723-G-C

76624422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17189723-G-T

76624429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17189716-G-A

76624429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17189716-G-C

76624429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17189716-G-T

http://identifiers.org/hco/9/GRCh38#76624462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/3/GRCm39#17189682-C-A

76624462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17189682-C-G

76624462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17189682-C-T

76624464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17189680-G-A

76624464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 17189680-G-C

76624464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 17189680-G-T

76624474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17189670-T-A

76624474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17189670-T-C

http://identifiers.org/hco/9/GRCh38#76624500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17189644-C-A

76624500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17189644-C-G

76624500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17189644-C-T

76624545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17189584-G-A

76624545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17189584-G-C

76624545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17189584-G-T

76624989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17189109-G-A

76624989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17189109-G-T

http://identifiers.org/hco/9/GRCh38#76625048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/3/GRCm39#17189050-C-A

76625048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17189050-C-T

76625053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 17189045-T-C

76625305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17188977-T-C

76625616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17188833-A-G

76625707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17188745-G-A

76625842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17188633-A-G

76625842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17188633-A-T

76625976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17188514-G-C

76626124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17188220-T-C

76626810-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17187881-A-T

http://identifiers.org/hco/9/GRCh38#76626859-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17187833-A-C

http://identifiers.org/hco/9/GRCh38#76627000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17187708-C-A

76627000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17187708-C-T

76627036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17187613-C-G

76627142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17187464-C-T

76627751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17186777-T-C

76627766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17186762-G-A

76627766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 17186762-G-T

76627859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17186670-A-G

http://identifiers.org/hco/9/GRCh38#76627916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17186625-C-A

76627916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17186625-C-T

http://identifiers.org/hco/9/GRCh38#76627957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17186590-C-A

76627957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17186590-C-G

76627957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17186590-C-T

76628324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17186266-G-A

76628357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17186231-G-A

http://identifiers.org/hco/9/GRCh38#76628386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17186203-A-C

76628386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17186203-A-G

http://identifiers.org/hco/9/GRCh38#76628457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17186129-C-A

76628541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17186051-T-C

76628541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17186051-T-G

76629230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17185653-G-A

76629230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17185653-G-T

76629292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 17185591-T-A

76629292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 17185591-T-C

76629297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 17185586-A-G

76629300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17185583-A-G

76629300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17185583-A-T

76629317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17185565-T-A

76629317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17185565-T-C

76629317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17185565-T-G

http://identifiers.org/hco/9/GRCh38#76629341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17185542-C-A

76629341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17185542-C-T

http://identifiers.org/hco/9/GRCh38#76629363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17185520-C-A

http://identifiers.org/hco/9/GRCh38#76629373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17185510-C-A

http://identifiers.org/hco/9/GRCh38#76629379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17185504-C-A

76629379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17185504-C-T

76630061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17184173-A-G

76630231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17184035-C-T

76630285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17183981-G-T

76630387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17183879-G-A

76631058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17183490-T-C

76631084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17183467-G-A

76635851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17179779-T-C

http://identifiers.org/hco/9/GRCh38#76636368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17179200-C-A

76636509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17179052-G-A

76636509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17179052-G-T

http://identifiers.org/hco/9/GRCh38#76636552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17179009-C-A

76636553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17179008-T-C

http://identifiers.org/hco/9/GRCh38#76636554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17179007-C-A

76636554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17179007-C-G

76636554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 17179007-C-T

76636565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 17178996-G-A

76636565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 17178996-G-T

76636599-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17178961-T-A

http://identifiers.org/hco/9/GRCh38#76636614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17178957-A-C

76637089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17178367-C-T

http://identifiers.org/hco/9/GRCh38#76637425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17177267-C-A

76637425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17177267-C-G

76637425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17177267-C-T

76637429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17177263-C-G

76637429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17177263-C-T

http://identifiers.org/hco/9/GRCh38#76637457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17177235-A-C

http://identifiers.org/hco/9/GRCh38#76637600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17177081-A-C

76637600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17177081-A-G

76637600-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17177081-A-T

76637604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17177077-T-C

76637684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176999-A-G

76637917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176812-A-G

76637960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176769-G-A

76638049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176700-T-C

76638122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176627-G-A

76638122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176627-G-T

76638144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176604-A-G

76638174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176589-A-G

76638192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17176571-A-G

76638360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176403-T-A

http://identifiers.org/hco/9/GRCh38#76638378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17176385-A-C

76638378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176385-A-G

76638417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176344-G-A

76638417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176344-G-T

76638442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176319-G-A

76638864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176014-G-A

76638864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17176014-G-T

76638892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17175965-C-T

76639759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17175780-G-A

76639815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17175723-G-A

76639821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17175717-A-G

76640263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17175137-T-C

76640543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17174884-G-A

76640577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17174849-C-T

76641001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17174501-G-A

76641216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17174363-A-G

76641464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17174035-T-A

76641684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17173601-C-T

76641810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17173450-T-A

76641810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17173450-T-C

76641810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17173450-T-G

76641862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17173397-G-T

76641945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17173320-G-C

76641953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17173312-A-G

76642046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17173233-T-A

http://identifiers.org/hco/9/GRCh38#76642072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17173207-C-A

76642072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17173207-C-T

76642177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17173096-T-C

76643182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17172125-G-A

76643351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17171942-C-T

http://identifiers.org/hco/9/GRCh38#76643395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#17171886-A-C

76643643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17171676-G-T

76643654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17171665-A-G

76644003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17171239-G-A

76644983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17170558-A-T

76645450-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17170189-T-A

76645450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17170189-T-C

76645472-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17170167-G-C

76646331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17169402-C-T

76646443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17169285-T-C

76646839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 17168914-T-C

76650519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17158477-T-C

76650624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17158343-T-C

76651039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 4203
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 17157917-G-A