109996387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53116702-T-G

109996594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53116872-A-T

109996762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53117021-G-A

109996897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53117205-C-T

109997156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53117454-G-A

109997221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53117519-A-G

http://identifiers.org/hco/10/GRCh38#109997365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53117661-C-A

109997365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53117661-C-T

109997375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53117671-G-T

http://identifiers.org/hco/10/GRCh38#109997401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53117696-C-A

109997401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53117696-C-T

109997456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53117747-T-G

109997510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53117768-T-C

109998200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53118708-G-A

http://identifiers.org/hco/10/GRCh38#109998296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53118805-C-A

http://identifiers.org/hco/10/GRCh38#109998334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53118836-A-C

http://identifiers.org/hco/10/GRCh38#109998352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53118854-A-C

109998519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53119037-G-A

109998918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53119440-G-T

109998970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53119495-T-G

109999074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53119594-G-A

109999363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53119935-T-C

109999424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53120096-G-C

109999574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53120451-T-C

110000218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53120942-C-T

110000345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53121018-A-G

http://identifiers.org/hco/10/GRCh38#110000353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53121026-A-C

110000698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53121322-G-T

110000731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53121355-G-A

110001489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53122126-T-C

110001754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53122346-A-G

110001924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53122711-T-C

110001975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53122762-T-C

http://identifiers.org/hco/10/GRCh38#110001996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53122783-A-C

110002583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53124532-T-C

110002928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53124862-A-G

110002928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53124862-A-T

110003071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125005-C-T

110003108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125041-G-A

110003127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125060-C-T

110003240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125171-A-G

110003334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53125285-T-C

110003334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53125285-T-G

http://identifiers.org/hco/10/GRCh38#110003378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53125450-A-C

110003380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53125452-C-T

110003431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53125503-T-C

110003573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125637-G-A

110003614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53125670-T-G

110004622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53127717-T-C

110005003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53128091-T-C

110005368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53128445-A-G

110005536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53128584-A-G

http://identifiers.org/hco/10/GRCh38#110005748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53128758-C-A

110005836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53128859-G-A

110005836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53128859-G-C

110005836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53128859-G-T

http://identifiers.org/hco/10/GRCh38#110005895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#53128933-C-A

110005895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53128933-C-T

110005908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53128948-A-G

http://identifiers.org/hco/10/GRCh38#110005952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53128991-C-A

110005952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53128991-C-G

110005952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53128991-C-T

110006020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53129033-G-A

110006020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53129033-G-T

110006208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53129201-G-A

110006208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53129201-G-T

110006779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53129802-G-A

110006937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53129962-C-G

110007385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53130428-G-A

110007386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53130429-G-A

110007460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53130507-G-C

110007489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53130538-C-T

110007556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53130605-G-C

110007587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53130623-C-G

110007608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53130644-A-G

http://identifiers.org/hco/10/GRCh38#110007663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53130698-C-A

110007693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53130728-G-A

http://identifiers.org/hco/10/GRCh38#110007702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#53130737-C-A

110007703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53130738-G-C

http://identifiers.org/hco/10/GRCh38#110007721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53130757-C-A

110007721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53130757-C-T

110007779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53130815-A-T

110007826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53130976-C-T

110007854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53131083-G-A

110007917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53131160-G-A

110007930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53131175-G-A

110007948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53131191-C-T

110007965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53131208-G-A

110007988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53131231-C-T

110008017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53131260-G-C

110008017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53131260-G-T

110008124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53131360-A-G

110008124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53131360-A-T

110008138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53131374-A-G

110008138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53131374-A-T

http://identifiers.org/hco/10/GRCh38#110008144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53131379-C-A

110008144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53131379-C-G

http://identifiers.org/hco/10/GRCh38#110008161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#53131396-C-A

110008265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53131494-G-A

110008265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53131494-G-T

110008331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53131551-C-T

http://identifiers.org/hco/10/GRCh38#110008432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53131569-C-A

110008432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53131569-C-T

110008434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53131571-A-T

http://identifiers.org/hco/10/GRCh38#110008482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#53131618-C-A

110008482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53131618-C-T

110008513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53131647-A-T

http://identifiers.org/hco/10/GRCh38#110008643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53131763-C-A

110008643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53131763-C-G

110008643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53131763-C-T

110008739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53131840-G-A

110008862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53132010-A-G

110008910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53132069-G-C

110009227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53132392-A-G

110009457-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53132602-T-A

110009898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53132993-A-G

110009919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53133013-A-T

110009924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53133018-T-G

110009929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53133027-T-G

110010037-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53133130-G-C

110011511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53133378-A-T

110011787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53133661-G-A

110011966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53133812-C-T

110012013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53133855-C-T

110012594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53134527-G-A

110012594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53134527-G-T

110013062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53135082-C-T

110013764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53136362-G-T

110015364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53137132-A-G

http://identifiers.org/hco/10/GRCh38#110015716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53137384-C-A

110015789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53137442-T-C

110016164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53137886-G-A

110016290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53138015-A-G

http://identifiers.org/hco/10/GRCh38#110016440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53138160-C-A

110016825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53138430-C-T

110016858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53138462-C-G

110017016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53138637-G-T

110017222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53138819-G-A

110017228-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53138825-T-A

110017584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53139286-G-A

110017600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53139517-T-C

http://identifiers.org/hco/10/GRCh38#110018592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53140634-C-A

110018596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53140638-G-C

110018603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53140645-C-T

110020085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53141241-T-G

110020738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53141991-C-G

110020970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53142181-T-C

110021011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53142209-A-G

110021070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53142277-C-T

110021105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53142311-G-C

110021105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53142311-G-T

110021233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53142434-C-G

110021376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53142590-G-C

110021435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53142627-T-C

http://identifiers.org/hco/10/GRCh38#110021639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53142759-A-C

110021639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53142759-A-G

110021848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53142920-T-C

110022113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53143172-C-T

110022167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53143198-G-A

110022167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53143198-G-T

110022226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53143259-T-C

110022486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53143508-A-G

110022867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53144777-G-T

110023058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53144955-G-A

110023231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53145161-G-A

110023241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53145171-A-G

110023245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53145175-G-C

110023297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53145219-C-T

110023551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53145431-C-T

110023570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53145445-T-A

110024238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53145784-T-C

110024278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53145824-A-T

110024497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53146089-G-A

110025863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53148071-A-T

110025867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53148075-C-T

110029499-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53149781-G-C

110029508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53149790-T-C

110030883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53151669-A-G

110030921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53151696-C-T

110030972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53151748-G-A

110031729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53151983-T-C

110031758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53151998-A-T

110031883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53152159-T-C

110031903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53152178-A-G

110032065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53152403-T-C

110032073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53152411-G-A

110032149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53153079-T-C

110032314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53153237-G-A

110032358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53153279-G-A

http://identifiers.org/hco/10/GRCh38#110032702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53153648-A-C

110032785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53153739-C-T

110032926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53153869-T-C

110032979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53153921-A-G

110033012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53153953-G-C

110033020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53153965-G-A

110033024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53153969-G-A

110033544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53154489-G-C

110033752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53154703-G-T

110034125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53155281-A-G

http://identifiers.org/hco/10/GRCh38#110034182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53155337-C-A

110034513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53155815-G-A

http://identifiers.org/hco/10/GRCh38#110034633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53156595-A-C

110034752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53156723-A-G

110034771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53156742-A-T

110034774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53156745-A-T

110034999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53156963-A-G

110035019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53156983-G-A

110035180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53157144-T-A

110035180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53157144-T-C

110035360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53157312-A-T

110040182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53158293-A-T

110040224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53158342-T-C

110040318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53158452-A-G

110040567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53158863-C-T

110040908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53159193-C-T

110041019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53159266-A-T

110041247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53159373-A-G

110041378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53159487-G-T

110041432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53159523-C-T

110041589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53159641-G-A

110041589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53159641-G-T

110041637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53159696-T-C

http://identifiers.org/hco/10/GRCh38#110041708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53159761-C-A

110041708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53159761-C-T

110041709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53159762-T-G

110053185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53161251-C-T

110053468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53161491-C-T

110053762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53162009-A-G

110053991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53162210-A-G

110054403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53162633-A-G

110055135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53162733-A-G

110055379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53163011-G-A

110055594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53163220-A-G

110055639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53163244-C-T

110055640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53163245-A-G

110055689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53163295-T-C

110055888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53163407-A-G

110055963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53163489-G-T

http://identifiers.org/hco/10/GRCh38#110056154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53163787-C-A

110056238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53163858-A-G

110056289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53163907-G-T

110056290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53163908-C-T

110056538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53164616-T-C

110056579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53164652-G-C

110056589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53164677-A-T

110056711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53164792-A-G

110057171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53165201-C-T

110057284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53165308-A-G

110057345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53165369-G-A

http://identifiers.org/hco/10/GRCh38#110057653-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53168105-A-C

110057653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53168105-A-G

110058402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53168975-C-G

110058402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53168975-C-T

110058432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53169010-A-G

110058456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53169048-A-G

http://identifiers.org/hco/10/GRCh38#110058499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53169103-A-C

110058573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53169171-C-G

110059822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53169772-G-A

110066764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53172623-T-C

110066881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53172806-C-T

110066883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53172808-T-A

110067071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53172974-T-C

110067071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53172974-T-G

110067172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53173080-A-G

110067172-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53173080-A-T

110067266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53173223-C-T

110067294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53173251-T-C

110067376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53173420-C-T

110067560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53173581-A-G

110067713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53173733-C-T

110067736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53173760-G-A

http://identifiers.org/hco/10/GRCh38#110067827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53173841-A-C

110067827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53173841-A-G

110068133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53174108-T-C

110068165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53174144-C-G

110068636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53174293-C-T

110068699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53174351-G-A

110068699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53174351-G-T

110069261-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53174625-T-G

110069284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53174651-T-A

110069720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53175056-G-A

110069720-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53175056-G-C

110069810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53175167-T-A

110070007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53175360-T-A

110070007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53175360-T-C

110070086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53175439-C-T

110070192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53175500-C-G

http://identifiers.org/hco/10/GRCh38#110070250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53175555-C-A

110070356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53175678-G-A

110070452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53175779-T-A

110070500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53175822-T-C

110070748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53176028-G-A

http://identifiers.org/hco/10/GRCh38#110070807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53176085-A-C

110071723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53176893-T-C

110071739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53176909-A-G

110071875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53177023-G-A

110072016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53177329-C-T

110072545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53177504-A-G

110072546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53177505-G-A

110072562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53177515-T-G

110073060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53178010-A-T

110073080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53178030-T-C

110074428-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53179195-G-C

110074445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53179212-A-G

110074473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53179239-A-G

110074543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53179304-C-G

110074543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53179304-C-T

110074570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53179333-A-G

110074570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53179333-A-T

110074607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53179359-A-G

http://identifiers.org/hco/10/GRCh38#110074679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53179438-C-A

110074679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53179438-C-T

110075086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53180036-T-G

110075137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53180118-G-T

110075192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53180170-G-A

110075239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53180217-T-C

110075270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53180248-A-G

110075351-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53180314-T-A

110075441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53180399-C-T

110075448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53180406-T-C

110075534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53180492-C-T

110075705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53180666-A-T

110075820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53180779-A-G

110076136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53181107-A-G

110076254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53181218-G-A

110076375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53181354-G-A

110076391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53181370-T-A

110077058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53182823-A-G

110077058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53182823-A-T

110077256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53183012-A-G

110077256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53183012-A-T

110077311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53183051-C-T

110077480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53183218-G-A

110077480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53183218-G-T

110077939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53183684-G-A

110078155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53183898-C-G

110078292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53184016-T-C

110078390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53184107-T-C

110078391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53184108-G-C

110078586-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53184288-G-C

110078634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53184338-C-T

110078676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53184379-G-A

110078795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53184493-G-A

http://identifiers.org/hco/10/GRCh38#110079237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53184941-C-A

110079930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53185455-A-G

110080086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53185587-A-G

110080303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53185793-T-A

110080483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53186005-T-G

110080798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53186315-G-A

110080993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 53186484-A-T

110081121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53186584-G-C

110081121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53186584-G-T

http://identifiers.org/hco/10/GRCh38#110081158-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53186621-A-C

110081484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53186993-A-G

110081791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53187285-C-T

110082005-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53187541-T-A

http://identifiers.org/hco/10/GRCh38#110082379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53187904-A-C

110082439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53187966-T-C

110082687-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53188630-T-A

110082801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53188702-T-C

110082817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53188718-C-G

110082960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53188838-T-C

110083151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53188954-A-G

110083193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53189001-G-A

110083706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53189500-G-C

110083815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53189608-G-C

110083826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53189619-C-G

http://identifiers.org/hco/10/GRCh38#110083919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53189706-C-A

http://identifiers.org/hco/10/GRCh38#110084421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#53190136-A-C

110084421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 53190136-A-G

110084485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53190237-C-G

110084513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53190262-G-C

http://identifiers.org/hco/10/GRCh38#110084657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53190393-A-C

http://identifiers.org/hco/10/GRCh38#110085209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53190853-C-A

110085209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53190853-C-T

110085357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53191005-A-T

110087351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53192423-G-C

110087402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53192481-A-G

http://identifiers.org/hco/10/GRCh38#110087485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53192558-C-A

110087734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53192786-G-C

110088057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53193085-C-G

110088388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53194568-A-G

110088454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53194663-A-G

110088457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53194666-A-G

110088486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53194694-G-A

110088954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53195739-T-C

110088962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53195747-A-G

110089021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53195801-A-G

110089021-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53195801-A-T

110089273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53196276-T-C

http://identifiers.org/hco/10/GRCh38#110089317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53196318-A-C

110089434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53196405-G-A

110089434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53196405-G-T

110093379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53197026-A-G

110093420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53197059-C-T

110093588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53197197-T-A

110093760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53197360-T-A

110093760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53197360-T-G

110093819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53197426-G-A

http://identifiers.org/hco/10/GRCh38#110094571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53198189-C-A

http://identifiers.org/hco/10/GRCh38#110094573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53198191-C-A

110095212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53198730-A-G

110099774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53200355-C-T

http://identifiers.org/hco/10/GRCh38#110100490-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53204755-A-C

110100528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53205143-A-G

http://identifiers.org/hco/10/GRCh38#110100674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53205272-A-C

110100824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53205422-A-G

110100900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53205494-A-G

http://identifiers.org/hco/10/GRCh38#110100957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53205531-A-C

110100957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53205531-A-G

110100957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53205531-A-T

110101060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53205621-T-A

110101272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53205857-T-C

http://identifiers.org/hco/10/GRCh38#110101411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53205922-C-A

110101411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53205922-C-T

110101441-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53205944-C-G

110101491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53206009-T-C

110102025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53206523-C-T

110102630-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53206741-T-A

http://identifiers.org/hco/10/GRCh38#110102787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53206872-A-C

110102787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53206872-A-G

110105668-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53208935-T-G

110105731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53209001-G-A

110105773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53209007-C-T

110105816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53209039-C-G

110106159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53209384-T-C

110106280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53209515-A-G

110106680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53210985-C-G

110107002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53211293-G-A

http://identifiers.org/hco/10/GRCh38#110107135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53211394-A-C

110107137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53211396-T-C

110107199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53211458-C-T

110107222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53211481-T-C

110107468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53211727-T-C

110107669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53211876-C-T

110107714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53211919-G-T

110107791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53211996-G-A

110107843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53212016-G-A

110107893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53212073-T-G

110112491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53214791-G-A

110112491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53214791-G-T

110112605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53214868-G-A

110112640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53214884-T-G

110112663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53214907-G-A

110113647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53217162-G-A

110113839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53217354-T-A

110113850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53217365-T-C

110113854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53217369-A-G

110113854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53217369-A-T

http://identifiers.org/hco/10/GRCh38#110113904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53217417-A-C

110113911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53217424-G-A

110113918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53217431-T-C

110113918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53217431-T-G

110113954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53217452-A-G

110114016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53217476-G-C

http://identifiers.org/hco/10/GRCh38#110114074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53217503-C-A

110114074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53217503-C-T

110114241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53217664-G-A

110114570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53218254-C-T

110115729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53219106-A-G

110115831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53219186-C-T

110116086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53219437-A-G

110116164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53219516-G-T

http://identifiers.org/hco/10/GRCh38#110116174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53219526-C-A

110116244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53219596-T-A

110116245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53219597-T-C

110116250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53219602-C-T

110116371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53219723-C-T

http://identifiers.org/hco/10/GRCh38#110116400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53219752-C-A

110116400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53219752-C-G

110116537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53219871-A-G

110116675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53219973-G-T

110117441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53220653-G-A

110117441-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53220653-G-C

110117452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53220664-T-C

110117457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53220669-G-T

110117522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53220686-G-A

110117661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53220766-G-A

http://identifiers.org/hco/10/GRCh38#110118073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53220954-C-A

110118073-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53220954-C-G

110118080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53220961-C-G

110118114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53220993-A-G

110118129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221007-C-T

110118146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221022-T-G

http://identifiers.org/hco/10/GRCh38#110118158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53221036-C-A

110118215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221087-G-A

110118449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221331-G-T

110118465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221347-A-G

110118510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221378-A-G

http://identifiers.org/hco/10/GRCh38#110118547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53221418-C-A

110118547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221418-C-T

110118548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221419-G-A

110118548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221419-G-T

110118613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53221483-G-T

110118664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 53221534-C-T

110118736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 53221606-T-C

110118736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 53221606-T-G

110118806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221660-G-A

110118806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221660-G-C

110118807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221661-A-G

110118821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221675-G-A

110118821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221675-G-T

110119069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221886-G-A

110119069-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221886-G-C

110119069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221886-G-T

110119099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221912-T-C

110119099-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53221912-T-G

http://identifiers.org/hco/10/GRCh38#110119297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53222090-A-C

110119365-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222158-G-C

110119375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222168-A-G

110119513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53222303-A-T

110119574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53222365-A-G

110119580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53222371-C-T

110119648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53222432-T-C

http://identifiers.org/hco/10/GRCh38#110119765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53222529-C-A

110119765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222529-C-T

http://identifiers.org/hco/10/GRCh38#110119799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53222562-C-A

110119799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222562-C-T

110119907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222643-G-A

110119933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222660-G-A

110119994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222716-G-A

110120016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222729-C-T

110120017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53222730-A-T

110122079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53223182-G-A

110122080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53223183-T-C

110122384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53223489-T-C

http://identifiers.org/hco/10/GRCh38#110122386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53223491-C-A

110122425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53223530-A-G

110122450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53223550-A-G

110122467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53223559-C-T

110122857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53223887-C-T

110123074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224081-A-G

110123177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224300-T-C

110123322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224454-A-G

110123349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224480-T-C

110123655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224757-G-A

110123673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224775-C-T

110123728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224820-A-G

110123798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224849-T-A

110123803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224854-A-G

110123803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53224854-A-T

http://identifiers.org/hco/10/GRCh38#110123857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53224908-C-A

110123865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53224916-C-T

110123908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53224921-T-C

110123908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53224921-T-G

110123941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53224958-T-C

110123941-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53224958-T-G

http://identifiers.org/hco/10/GRCh38#110123945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53224962-A-C

110123972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53224980-T-C

110123995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53225003-A-G

110123995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53225003-A-T

110124037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53225045-T-G

110124070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53225078-G-A

110124100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53225108-T-C

110124109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53225117-T-C

http://identifiers.org/hco/10/GRCh38#110124310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53225319-A-C

110124310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225319-A-G

110124310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225319-A-T

110124319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225328-C-G

110124319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225328-C-T

110124322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225331-G-C

110124331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225340-G-C

110124331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225340-G-T

110124336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225345-G-T

http://identifiers.org/hco/10/GRCh38#110124379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53225387-A-C

110124379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225387-A-T

110124386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225399-T-A

110124386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225399-T-C

110124569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225610-G-A

110124659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225819-T-C

110124733-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225896-A-T

110124744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53225907-G-C

110125356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53226382-A-G

110125601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53226610-T-C

110125675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53226685-T-C

110125773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53226774-A-G

110125773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53226774-A-T

110125921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53226929-T-C

110125921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 53226929-T-G

110125955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53226963-G-C

110125955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53226963-G-T

110125956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53226964-G-A

110125957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53226965-T-C

110126010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227503-G-T

110126288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227724-A-G

110126306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227742-G-A

110126306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227742-G-T

http://identifiers.org/hco/10/GRCh38#110126310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53227746-C-A

110126310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227746-C-G

110126310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227746-C-T

110126315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227751-A-T

http://identifiers.org/hco/10/GRCh38#110126316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53227752-C-A

110126316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227752-C-T

110126326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227761-G-A

110126326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227761-G-T

110126356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227788-A-G

110126437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53227858-T-C

110126519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227938-A-G

110126537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227954-T-C

110126556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53227983-A-G

http://identifiers.org/hco/10/GRCh38#110126643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53228049-C-A

110126643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53228049-C-T

110126699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53228082-G-A

110127201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53228492-G-A

110127201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53228492-G-C

110130227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53230752-T-A

110130227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53230752-T-G

http://identifiers.org/hco/10/GRCh38#110130269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53230827-C-A

110130269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53230827-C-G

110130290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53230848-A-G

110130293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53230851-G-A

110130437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 53231009-A-G

110131152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53231482-T-C

110131190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53231520-G-C

110131285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53231765-T-G

110131322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53231801-T-C

http://identifiers.org/hco/10/GRCh38#110131323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53231802-C-A

110131750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53232223-A-G

110132032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53232484-T-A

110132129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53232577-C-T

110132148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53232595-A-G

http://identifiers.org/hco/10/GRCh38#110132165-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53232612-C-A

110132343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53232779-G-A

110132343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53232779-G-T

110132412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53232848-A-G

110132446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53232880-A-G

110132459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53232890-G-A

110132478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53232895-G-T

http://identifiers.org/hco/10/GRCh38#110132570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53232955-C-A

110132570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53232955-C-G

110132570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53232955-C-T

110132614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53233011-G-A

110132614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53233011-G-T

http://identifiers.org/hco/10/GRCh38#110132620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53233017-C-A

110132620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53233017-C-T

110132624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53233021-G-A

110132624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53233021-G-T

110133068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53233170-A-G

110133228-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53233313-A-T

110133237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53233326-T-C

http://identifiers.org/hco/10/GRCh38#110133245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53233334-C-A

110133268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53233356-G-A

110133268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53233356-G-T

110133298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53233406-A-G

110133321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53233424-C-T

http://identifiers.org/hco/10/GRCh38#110133361-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53233464-A-C

110133361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: missense variant
orthologous variants: 53233464-A-G

110133361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: missense variant
orthologous variants: 53233464-A-T

http://identifiers.org/hco/10/GRCh38#110133366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53233469-A-C

110133367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: missense variant
orthologous variants: 53233470-G-T

110133726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: 53233827-G-A

110133803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: 53233916-A-G

110133842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: 53233953-T-A

110133861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: 53233976-T-C

110133878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: 53233993-A-G

110133906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: 53234017-A-G

http://identifiers.org/hco/10/GRCh38#110133920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53234030-A-C

110133920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: 53234030-A-G

110133941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: 53234051-C-T

http://identifiers.org/hco/10/GRCh38#110134064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53234159-A-C

http://identifiers.org/hco/10/GRCh38#110134528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53234574-A-C

http://identifiers.org/hco/10/GRCh38#110134836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53234812-C-A

110134836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: 53234812-C-T

110134936-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: 53234927-T-G

http://identifiers.org/hco/10/GRCh38#110135121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53235105-C-A

110135241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: 53235198-C-T

http://identifiers.org/hco/10/GRCh38#110135322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#53235278-A-C

110135322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 245
most severe consequence: 3 prime UTR variant
orthologous variants: 53235278-A-G