107791010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53725427-A-G

107791010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53725427-A-T

http://identifiers.org/hco/11/GRCh38#107791226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53725187-C-A

107791231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53725182-G-T

107791334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53725053-T-C

http://identifiers.org/hco/11/GRCh38#107791336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53725051-C-A

107791501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724908-T-C

107791525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724884-G-T

107791549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724866-T-A

107791549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724866-T-C

107791985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724794-A-G

107792045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724737-T-A

107792045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724737-T-C

107792045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724737-T-G

107792075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724708-G-T

107792092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724691-T-C

107792092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724691-T-G

http://identifiers.org/hco/11/GRCh38#107792112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53724675-C-A

107792114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724673-C-T

107792118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724669-G-T

107792144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724629-G-A

http://identifiers.org/hco/11/GRCh38#107792183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53724602-C-A

http://identifiers.org/hco/11/GRCh38#107792201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53724584-A-C

107792201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724584-A-G

107792201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724584-A-T

107792379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724487-A-T

http://identifiers.org/hco/11/GRCh38#107792504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53724363-C-A

107792504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724363-C-T

107792512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3 prime UTR variant
orthologous variants: 53724355-T-G

107792721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 53724144-G-A

107792721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 53724144-G-T

107792747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, synonymous_variant
orthologous variants: 53724118-C-T

107792828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53724037-G-C

107792856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53724009-T-C

http://identifiers.org/hco/11/GRCh38#107792869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53723996-C-A

107792869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53723996-C-G

107792878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53723987-G-A

107792878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53723987-G-T

107793106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53723849-G-A

107793106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53723849-G-T

107793382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53723632-C-T

http://identifiers.org/hco/11/GRCh38#107793769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53723310-C-A

107793769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53723310-C-T

107793975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53722971-T-C

107793984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53722963-A-G

http://identifiers.org/hco/11/GRCh38#107794034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53722910-A-C

107794066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53722883-A-G

107794096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53722816-T-C

107794101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53722811-G-A

107794101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53722811-G-T

107794115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53722797-C-T

107794127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53722785-C-G

107794148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53722780-T-C

107794168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53722756-C-T

107794171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53722751-C-T

http://identifiers.org/hco/11/GRCh38#107794203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53722720-C-A

107794223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53722701-A-G

107797857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53721914-T-A

107797857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53721914-T-G

107797889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53721882-G-A

107797889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53721882-G-T

107798081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53721819-G-T

107798249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53721734-T-C

107798619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53721382-C-T

107799273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53720821-T-C

http://identifiers.org/hco/11/GRCh38#107800218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53719504-C-A

107800218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53719504-C-T

107802581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53719079-A-G

107802862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53718844-G-A

107802862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53718844-G-T

http://identifiers.org/hco/11/GRCh38#107802873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53718826-C-A

107802907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53718752-A-G

107802978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53718334-T-C

107802978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53718334-T-G

107803038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 53718274-T-C

107803258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53718062-A-G

107803415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53717939-G-A

107803415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53717939-G-T

107803418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53717936-T-G

107803422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53717932-A-G

107803569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53717779-T-C

107803569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53717779-T-G

107803641-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53717708-T-G

107803758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53717601-T-C

http://identifiers.org/hco/11/GRCh38#107804227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53717455-A-C

107804273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53717413-T-C

107804513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53717190-G-A

107804585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53717129-A-G

107804675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53717070-T-C

107804804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53716934-A-T

107804905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53716832-A-G

http://identifiers.org/hco/11/GRCh38#107805368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53715475-C-A

107805368-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 53715475-C-G

107805368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 53715475-C-T

107805464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 53715379-T-C

107805530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53715313-G-A

107806708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53714068-C-T

http://identifiers.org/hco/11/GRCh38#107806894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53713881-C-A

107806894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53713881-C-G

107808006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53712973-G-C

http://identifiers.org/hco/11/GRCh38#107808016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53712966-A-C

107808070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53712911-A-G

107808328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53712661-G-A

107808674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53711226-C-T

107809142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53710897-C-T

107809199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53710844-G-T

107809753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53710732-G-A

107810762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53710674-G-C

107810762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53710674-G-T

107810912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53710537-T-C

107811338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53708754-T-C

107811380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53708715-C-T

107811635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53708449-A-G

107811645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53708439-T-C

107811767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 53708320-T-C

http://identifiers.org/hco/11/GRCh38#107811828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53708259-C-A

107811828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53708259-C-T

107811886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53708205-T-C

107811886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53708205-T-G

107812944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53707619-A-G

107813167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53707465-G-A

107813227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53707401-C-T

107813522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53706372-G-A

107813613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53706282-C-T

107815760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53705325-T-C

107815768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53705317-A-G

107815776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53705309-C-T

107815831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, stop_gained
orthologous variants: 53705254-A-T

107815837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 53705248-T-C

107815924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 53705161-A-G

http://identifiers.org/hco/11/GRCh38#107815966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53705119-C-A

107815968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 53705117-A-G

http://identifiers.org/hco/11/GRCh38#107815972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53705113-A-C

107815972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 53705113-A-T

107815982-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53705104-G-T

107815986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53705100-T-A

http://identifiers.org/hco/11/GRCh38#107815987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53705099-C-A

107815987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53705099-C-G

107815987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53705099-C-T

107816100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53704413-T-C

107821082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53702553-T-C

107821124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53702512-G-A

107821124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53702512-G-C

107821190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53702446-T-C

107821536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53702104-C-T

107821566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53702083-A-G

107821583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53702068-A-G

http://identifiers.org/hco/11/GRCh38#107821671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53702004-C-A

107821671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53702004-C-T

107821683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53701992-T-C

107821698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53701977-G-T

107821935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53701763-C-T

107823081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53700588-C-T

107823219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53700442-C-T

107823242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53700420-A-G

107823316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53700350-T-A

107823322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53700344-T-C

107823356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53700308-G-T

107823608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53700090-A-G

107836038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53697333-A-G

107836554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53696729-A-G

107837227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53695894-C-T

107837237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53695884-T-C

107837290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53695822-T-A

107837337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53695770-G-C

107840303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53694551-T-G

107840336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53694516-C-T

107840424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53694426-A-G

107840499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53694359-C-T

http://identifiers.org/hco/11/GRCh38#107840636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53694241-C-A

107840672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 53694211-A-G

http://identifiers.org/hco/11/GRCh38#107840697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53694186-C-A

107840702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 53694181-G-A

107840702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 53694181-G-C

107840702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 53694181-G-T

107840733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 53694150-G-A

107840733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 53694150-G-T

107840736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 53694147-T-C

107840835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53694066-T-C

http://identifiers.org/hco/11/GRCh38#107840837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53694064-C-A

107840837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53694064-C-T

http://identifiers.org/hco/11/GRCh38#107840879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53694022-C-A

http://identifiers.org/hco/11/GRCh38#107840898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53694004-C-A

107840939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53693963-G-A

http://identifiers.org/hco/11/GRCh38#107841053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53693855-A-C

107841062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53693846-A-G

107841114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53693784-G-T

107845565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53691191-G-A

107845663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53691081-T-C

107846065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53690821-G-T

http://identifiers.org/hco/11/GRCh38#107847633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53687622-A-C

107848130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53686506-T-C

107848135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53686501-C-G

107848195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53686452-C-G

107848195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53686452-C-T

107848301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53686351-G-A

107848839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53684989-T-C

107848986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53684893-A-G

107849180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53684728-G-A

107849215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53684693-C-G

107849215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53684693-C-T

107849301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53684610-C-T

107849682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53684553-A-G

107849753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53684465-C-T

107851806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53683804-T-C

107851886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53683730-G-A

107851901-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53683715-T-A

107851901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53683715-T-G

http://identifiers.org/hco/11/GRCh38#107853130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53683101-A-C

107853212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53683060-T-C

107853427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53682798-G-A

107853771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -C-T

107854536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53682382-C-G

107854536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53682382-C-T

107854855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53681722-T-C

107854964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53681652-G-A

http://identifiers.org/hco/11/GRCh38#107854977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53681640-A-C

107855197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53681544-G-A

107855802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53680961-A-G

107857415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53680318-A-G

107857625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53680120-G-T

107858283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 53679514-G-A

107858416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53679383-T-A

107858416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53679383-T-C

107858456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53679343-G-A

107858456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53679343-G-C

107858456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 53679343-G-T

http://identifiers.org/hco/11/GRCh38#107858518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53679300-C-A

107858518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 53679300-C-T

107858522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 53679293-G-A

107858522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 53679293-G-T

107858548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 53679268-T-C

http://identifiers.org/hco/11/GRCh38#107858549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53679267-C-A

107858627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 53679202-A-G

107858714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 53679120-T-A

107858714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 53679120-T-C

107858854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5 prime UTR variant
orthologous variants: 53678980-G-A

107858854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5 prime UTR variant
orthologous variants: 53678980-G-T

107858886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5 prime UTR variant
orthologous variants: 53678936-C-T

107858891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5 prime UTR variant
orthologous variants: 53678931-T-C

107858891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5 prime UTR variant
orthologous variants: 53678931-T-G

107858918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5 prime UTR variant
orthologous variants: 53678905-T-C

107859674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron_variant, undefined
orthologous variants: 53678319-T-C

107859718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 53678278-C-T

107859872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron_variant, undefined
orthologous variants: 53678179-G-A

107859872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron_variant, undefined
orthologous variants: 53678179-G-T

107860011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron_variant, undefined
orthologous variants: 53678008-A-G

107860070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron_variant, undefined
orthologous variants: 53677946-A-G

107862675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53673522-G-A

107863021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53673185-T-C

107863861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53672434-G-A

107863883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53672410-G-A

107863883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53672410-G-T

107864139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53672152-G-A

107864197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53672107-G-A

107864287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53672055-T-C

107864324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53672021-T-C

107864390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53671967-G-A

107864390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53671967-G-T

107864454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53671915-G-C

http://identifiers.org/hco/11/GRCh38#107867500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53661192-C-A

107867500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53661192-C-T

http://identifiers.org/hco/11/GRCh38#107867809-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53660895-A-C

107868455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53660563-C-G

http://identifiers.org/hco/11/GRCh38#107868567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53660513-C-A

107868567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53660513-C-T

107868655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53660436-C-T

107868656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53660435-C-T

107869640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53660058-C-T

107869662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53660038-A-G

107869736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53659978-T-C

107869736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53659978-T-G

107888850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53651611-C-T

107888857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53651604-T-A

107888899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53651563-C-G

107889008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53651351-T-C

107889008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53651351-T-G

107889202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53651168-T-C

107890227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53650783-T-C

107890498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53650522-G-A

http://identifiers.org/hco/11/GRCh38#107890619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53649697-C-A

107890669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53649657-C-T

107890811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53649446-T-C

107891728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53648039-G-A

107893307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53647555-G-C

107895005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53645744-C-T

107895192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53645557-A-G

107895217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53645536-G-C

http://identifiers.org/hco/11/GRCh38#107895248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53645505-C-A

107895248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53645505-C-T

http://identifiers.org/hco/11/GRCh38#107895285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53645477-C-A

107906502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53632486-T-G

107906660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53632325-T-C

107906856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53632130-C-T

107906903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53632076-A-G

107917635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron_variant, undefined
orthologous variants: 53621923-G-C

107917725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron_variant, undefined
orthologous variants: 53621853-G-T

107925754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53619377-G-A

http://identifiers.org/hco/11/GRCh38#107925893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53619238-C-A

107925927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53619204-A-G

107927365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53618278-G-T

http://identifiers.org/hco/11/GRCh38#107927427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#53618236-C-A

107927427-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53618236-C-G

107927427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron variant
orthologous variants: 53618236-C-T

107928100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron_variant, undefined
orthologous variants: 53618049-G-A

107928100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: intron_variant, undefined
orthologous variants: 53618049-G-T

107928202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5 prime UTR variant
orthologous variants: 53617945-G-T

107928234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53617912-G-A

107928234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53617912-G-C

107928234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53617912-G-T

http://identifiers.org/hco/11/GRCh38#107928248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#53617898-C-A

107928248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23615
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 53617898-C-T