104468935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133967237-G-T

104469015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133967160-T-C

104469069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133967110-A-G

104469417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133966776-A-G

104469512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133966675-G-T

104469527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133966660-A-T

104469545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133966642-A-G

104469609-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133966592-T-A

104469609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133966592-T-C

104469609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133966592-T-G

104469997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133966187-G-A

104470011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133966173-G-T

104470181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133965964-A-G

104470244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133965905-A-T

http://identifiers.org/hco/4/GRCh38#104470326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133965828-A-C

104470407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133965748-A-T

104470492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133965661-G-T

104470493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133965660-A-G

104470507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133965643-C-T

104470539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133965612-C-G

104470584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133965568-G-T

104470742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133965453-G-A

104470885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133965337-G-A

104470885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133965337-G-T

104470939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133965283-T-C

104471267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133964964-T-C

104471367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133964859-G-T

104471388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133964833-T-C

104471411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133964811-T-C

104471444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133964784-A-G

104471444-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133964784-A-T

104471663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133964562-A-G

http://identifiers.org/hco/4/GRCh38#104471759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133964466-C-A

104471759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133964466-C-T

http://identifiers.org/hco/4/GRCh38#104472032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133964176-C-A

104472032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133964176-C-T

104472195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133963983-G-A

104472195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133963983-G-C

104472195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 133963983-G-T

104472572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133963606-G-A

104472665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133963518-T-A

104472760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133963426-C-G

104472875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133963355-T-G

104472914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133963318-T-C

104472923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133963309-T-C

104472947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133963289-T-C

104472947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133963289-T-G

104472952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133963284-T-C

104473819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133962951-A-G

104473908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133962851-T-C

104473927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133962832-T-C

104474017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133962598-T-C

104474223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133962436-T-C

104474604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133961943-T-C

104474998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133961558-A-T

104475119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 133961420-G-T

104475322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133960699-C-T

104475483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133960519-T-C

104475792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133960220-G-C

104475792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133960220-G-T

104476169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133959908-T-G

104476340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133959750-A-G

http://identifiers.org/hco/4/GRCh38#104476748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133959231-A-C

104476894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133959084-C-T

104476895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133959083-G-A

http://identifiers.org/hco/4/GRCh38#104476925-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133959051-A-C

104477219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133958778-A-G

104477305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133958684-A-T

104477829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133958032-G-A

104478102-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133957771-G-C

104478226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133957657-G-A

104478293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133957612-C-G

104478357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133957556-T-C

104478428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133957493-T-C

104478550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133957388-C-T

104478632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133957317-G-A

http://identifiers.org/hco/4/GRCh38#104478811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133957126-A-C

104478987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956851-G-A

104479056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956741-T-C

104479061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956739-T-C

http://identifiers.org/hco/4/GRCh38#104479540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133956351-C-A

104479760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956127-C-T

104479763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956121-T-C

104479769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956115-C-G

104479771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956113-T-C

104479771-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956113-T-G

http://identifiers.org/hco/4/GRCh38#104479773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133956111-C-A

104479773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956111-C-T

104479774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956110-C-T

104479775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956109-C-T

http://identifiers.org/hco/4/GRCh38#104479777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133956107-C-A

http://identifiers.org/hco/4/GRCh38#104479781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133956103-C-A

104479787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956097-C-G

104479787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956097-C-T

104479794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956090-C-T

104479795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956089-C-T

104479799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956085-G-A

104479799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956085-G-C

104479799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956085-G-T

104479802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956082-C-T

104479819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956065-T-G

http://identifiers.org/hco/4/GRCh38#104479827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133956057-C-A

104479831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133956053-C-T

http://identifiers.org/hco/4/GRCh38#104480070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133955839-C-A

104480070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133955839-C-T

104480073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133955836-T-G

104480125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133955793-A-G

104480815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133955135-G-A

104481066-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133955000-A-T

104481068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133954998-A-G

104481572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133954833-T-C

104481572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133954833-T-G

104481856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133954574-T-C

104481919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133954516-T-G

104482061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133954400-C-T

104482100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133954367-A-G

104482226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133954239-A-G

104482237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133954228-G-A

104482237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133954228-G-C

104482246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133954201-A-G

104482353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133954092-A-G

104482399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133954046-C-T

104482645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133953838-C-T

104482646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133953837-G-A

104482949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133953555-C-T

104482959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133953547-G-T

104482982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133953521-T-C

104483070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133953439-T-C

104483128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133953384-T-C

104483336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133953190-C-T

104483531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133953056-T-C

104484481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133952626-G-A

104484733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133952390-A-G

104484801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133952322-C-G

104485533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133951631-G-A

104486032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133951137-T-C

104486097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133951056-T-C

104486139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133951015-A-G

104486170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950983-G-A

104486618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950481-G-C

104486668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950434-T-C

104486917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950172-G-A

http://identifiers.org/hco/4/GRCh38#104487021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133950062-A-C

104487077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133950011-G-A

http://identifiers.org/hco/4/GRCh38#104487141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133949940-A-C

104487451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949687-T-C

104487452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949686-A-G

104487453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949685-T-A

104487476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949662-T-A

104487552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949587-T-A

104487552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949587-T-C

104487895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949278-G-A

104487938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949236-C-T

104487956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949219-G-C

104488043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949128-T-G

104488087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949088-T-C

104488100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949078-G-T

104488107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133949066-G-T

104488413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133948823-A-G

104488567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133948663-C-T

104488650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133948592-G-A

104488650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133948592-G-C

http://identifiers.org/hco/4/GRCh38#104488745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133948490-C-A

104488745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133948490-C-T

104488877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133948343-A-G

104489033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133948162-C-T

104489161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133948022-G-A

104489492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133947722-T-G

http://identifiers.org/hco/4/GRCh38#104489729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133947502-C-A

104489938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133947303-T-C

104489975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133947266-A-G

104490146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133947102-T-C

http://identifiers.org/hco/4/GRCh38#104490221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133947022-A-C

104490221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133947022-A-G

104490224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133947019-T-G

104490341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133946891-G-A

104491225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 133945993-G-A

104491509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 133945712-G-A

104491509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 133945712-G-T

104491528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 133945693-T-C

104491744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 133945477-T-G

104491863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945358-G-A

104491863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945358-G-C

104491863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945358-G-T

104491880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945341-G-A

104491880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945341-G-T

104491887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945334-G-A

104491887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945334-G-C

104491887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945334-G-T

104491891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945330-G-A

104491891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945330-G-T

104491905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945316-G-A

104491905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945316-G-T

104491908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945313-G-A

104491908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 133945313-G-T

104492092-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945129-A-T

104492144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133945074-A-G

http://identifiers.org/hco/4/GRCh38#104492205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133945010-C-A

104492205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133945010-C-T

http://identifiers.org/hco/4/GRCh38#104492239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133944982-C-A

104492239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133944982-C-T

http://identifiers.org/hco/4/GRCh38#104492278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133944932-C-A

104492278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133944932-C-G

104492465-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133944743-G-C

104492465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 133944743-G-T

104492818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133944394-T-C

104493071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133944087-C-T

104493102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133944056-T-G

http://identifiers.org/hco/4/GRCh38#104493224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#133943931-A-C

104493234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133943921-C-T

104493449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133943713-T-G

104493540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133943621-G-A

104493613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133943549-C-T

104494361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942798-G-A

104494664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942483-G-A

104494664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942483-G-C

104494664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942483-G-T

104494665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942482-G-A

104494665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942482-G-C

104494665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 133942482-G-T

104494796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24593
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 133942349-G-T