62715594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 5 prime UTR variant
orthologous variants: 106099642-G-A

62715594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 5 prime UTR variant
orthologous variants: 106099642-G-C

62715594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 5 prime UTR variant
orthologous variants: 106099642-G-T

62715629-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106099683-T-A

62715629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106099683-T-C

62715663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106099713-G-A

62715663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106099713-G-C

62715663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106099713-G-T

62715680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106099730-T-C

http://identifiers.org/hco/18/GRCh38#62715692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#106099742-C-A

62715692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous_variant, undefined
orthologous variants: 106099742-C-G

62715692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous_variant, undefined
orthologous variants: 106099742-C-T

http://identifiers.org/hco/18/GRCh38#62715698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#106099748-C-A

62715698-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous_variant, undefined
orthologous variants: 106099748-C-G

62715698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous_variant, undefined
orthologous variants: 106099748-C-T

62715872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous_variant, undefined
orthologous variants: 106099868-G-A

62715872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous_variant, undefined
orthologous variants: 106099868-G-T

http://identifiers.org/hco/18/GRCh38#62716005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106099995-C-A

62716005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106099995-C-G

62716005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106099995-C-T

http://identifiers.org/hco/18/GRCh38#62716334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100309-C-A

62716334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100309-C-T

http://identifiers.org/hco/18/GRCh38#62716406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100381-C-A

62716406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100381-C-T

http://identifiers.org/hco/18/GRCh38#62716483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100444-C-A

62716483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense_variant, undefined
orthologous variants: 106100444-C-T

http://identifiers.org/hco/18/GRCh38#62716484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100445-C-A

62716484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous_variant, undefined
orthologous variants: 106100445-C-T

62716485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense_variant, undefined
orthologous variants: 106100446-G-A

62716485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense_variant, undefined
orthologous variants: 106100446-G-T

http://identifiers.org/hco/18/GRCh38#62716503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100464-C-A

62716518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106100475-T-A

62716518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106100475-T-C

62716558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106100515-G-A

62716558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106100515-G-T

http://identifiers.org/hco/18/GRCh38#62716637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100594-A-C

62716637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100594-A-G

62716637-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100594-A-T

62716676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100633-G-A

62716676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100633-G-T

62716691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100648-G-A

62716691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100648-G-C

62716691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100648-G-T

http://identifiers.org/hco/18/GRCh38#62716692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100649-C-A

62716692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106100649-C-T

62716698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106100655-G-A

62716698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106100655-G-T

http://identifiers.org/hco/18/GRCh38#62716718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100672-C-A

62716718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100672-C-G

62716718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100672-C-T

http://identifiers.org/hco/18/GRCh38#62716724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100678-C-A

62716724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100678-C-G

62716724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100678-C-T

http://identifiers.org/hco/18/GRCh38#62716751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100705-C-A

62716751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100705-C-G

62716751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100705-C-T

http://identifiers.org/hco/18/GRCh38#62716775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100729-C-A

62716775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100729-C-T

http://identifiers.org/hco/18/GRCh38#62716796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100753-C-A

62716796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100753-C-T

62716800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106100757-T-C

62716869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106100802-C-G

62716869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106100802-C-T

62716895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100828-C-T

http://identifiers.org/hco/18/GRCh38#62717037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100967-C-A

62717037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106100967-C-T

http://identifiers.org/hco/18/GRCh38#62717057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106100987-C-A

62717057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100987-C-G

62717057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106100987-C-T

http://identifiers.org/hco/18/GRCh38#62717124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106101042-C-A

62717124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106101042-C-T

62717204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106101122-G-A

http://identifiers.org/hco/18/GRCh38#62717270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#106101188-C-A

62717270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, undefined
orthologous variants: 106101188-C-G

62717310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106101230-G-A

62717310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106101230-G-C

62717310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106101230-G-T

62717367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106101251-G-A

62717425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, undefined
orthologous variants: 106101314-G-A

62717457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106101345-C-T

62717462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106101350-G-A

62717791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, undefined
orthologous variants: 106101706-C-T

62717807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106101721-A-T

62717863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106101785-C-T

62717895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, undefined
orthologous variants: 106101812-A-G

62718139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106102013-T-C

62718140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106102014-A-G

62718177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106102053-T-A

62718264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106102101-A-T

62718295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106102130-C-T

62718335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106102156-T-A

62718453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106102263-A-G

62718931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106102777-C-G

62718931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106102777-C-T

62719123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106102953-A-G

62719459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106103305-C-T

62719663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106103504-T-C

62719676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106103516-A-G

62720082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106103958-A-G

62720674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106104530-C-T

62720973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106104812-T-G

62721139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106104968-A-G

62721503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106105244-T-C

62721516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106105257-C-T

62721887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106105634-G-A

62721972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106105719-T-C

62722095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106105841-C-T

62722170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106105918-G-C

62722349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106106092-G-T

62722428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106106157-C-T

62722554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106106245-A-G

62722719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106106438-G-T

62722754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106106479-C-T

62722996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106106710-T-A

http://identifiers.org/hco/18/GRCh38#62723264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106106953-C-A

62723395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106107093-A-G

http://identifiers.org/hco/18/GRCh38#62723481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106107187-A-C

62723563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106107259-A-G

62723636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106107332-A-T

62723735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106107663-T-C

62723812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106107747-T-G

62724250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106108378-C-T

62724253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106108381-C-T

62724358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106108586-C-T

62724481-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106108809-T-G

http://identifiers.org/hco/18/GRCh38#62724596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106108891-C-A

62724818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106109095-G-A

62724903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106109184-G-T

62725683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106109910-G-T

62726119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106110267-C-T

62726142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106110290-G-A

http://identifiers.org/hco/18/GRCh38#62726344-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106110481-A-C

62726344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106110481-A-G

62726344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106110481-A-T

62727821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106110946-C-T

62728381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106111451-G-C

62728900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106111654-G-T

62729241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106112180-G-A

62730095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106113191-A-G

62733707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106113951-G-A

62733870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106114128-G-A

62733870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106114128-G-C

62734072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106114307-C-T

62734112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106114391-C-G

62734115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106114394-G-A

62734137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106114455-A-G

62734474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106115037-T-A

62734690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106115227-A-G

62735913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106115892-C-T

62735958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106115916-A-G

62736330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106116342-G-A

62736374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106116395-C-T

62736933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106116893-C-G

62736986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106116942-T-G

62737556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, undefined
orthologous variants: 106117565-C-T

62737665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, undefined
orthologous variants: 106117663-T-A

http://identifiers.org/hco/18/GRCh38#62737969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106118166-C-A

62737969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106118166-C-T

62739614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106119136-A-G

http://identifiers.org/hco/18/GRCh38#62739880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106119634-A-C

62739957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106119709-G-A

62739969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106119721-C-T

62740000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106119751-C-T

62740096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106119845-T-C

62740134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106119875-C-T

62740227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106119945-G-C

http://identifiers.org/hco/18/GRCh38#62741126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106120915-C-A

62741216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106121023-G-A

62741611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106121412-T-C

62741674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106121604-T-G

62741851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106121784-A-G

http://identifiers.org/hco/18/GRCh38#62741864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106121796-A-C

http://identifiers.org/hco/18/GRCh38#62741986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106121910-C-A

62742034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106121956-T-C

62742190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106122132-G-A

62744022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106122466-C-T

62744047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106122492-G-A

62744258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106122663-C-G

62744258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106122663-C-T

62744667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106123052-G-A

62744777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106123156-T-C

62745055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106123929-G-A

62745055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106123929-G-C

62745584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106124434-C-T

62750336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106126284-C-T

62750438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106126337-T-C

62750444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106126343-T-C

62750452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106126352-C-T

62750463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106126363-A-G

62750554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106126459-C-T

62750599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106126503-G-C

62750744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106126608-T-G

62750958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106126880-G-A

62750958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106126880-G-T

62753686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106129456-C-T

62754404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106130129-A-G

http://identifiers.org/hco/18/GRCh38#62754406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106130131-A-C

62754406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106130131-A-G

62754406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106130131-A-T

62754777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106130500-A-G

62755076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106130632-A-G

62756212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106130805-G-C

62756911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106131552-G-A

62756911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106131552-G-C

62757080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106131708-G-A

62757080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106131708-G-T

62757110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106131744-A-G

62757136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106131764-T-C

62757413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106132008-A-G

62757502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106132102-G-C

62757695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106132263-C-T

62757721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106132289-C-T

62757908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106132480-G-A

62757917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106132489-G-A

62759618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106134389-T-C

62759623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106134394-A-G

62759943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106134642-G-T

62760098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106134773-G-C

62760150-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106134819-T-C

62760151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106134820-T-A

62762741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106138061-T-C

http://identifiers.org/hco/18/GRCh38#62763040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106138307-C-A

62763040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106138307-C-T

62763330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106138938-G-A

62763386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106138990-G-C

62763433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106139031-C-G

62763437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106139035-G-A

62763437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106139035-G-T

62763587-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106139125-A-G

62766658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106141054-A-G

62767579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106141806-C-T

62768204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106147263-G-C

62768298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106147357-G-A

62768337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106147391-G-T

62768430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106147452-G-A

62768920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106147780-T-C

62768940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106147800-G-A

62777954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106148619-G-C

62777959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106148624-A-G

62778257-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106148901-A-T

62778707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106149545-T-C

http://identifiers.org/hco/18/GRCh38#62778769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106149605-A-C

62778817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106149654-G-A

62778949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106149782-A-G

62779117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106149947-T-C

62779136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106149966-C-T

62779306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106150143-A-G

62779376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106150213-T-C

62779450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 106150280-A-G

62779773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106150605-T-G

62780057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106150849-A-G

62780099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106150891-A-T

62780155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106150944-C-T

62780202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106150992-T-G

62780543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106152824-T-C

62780561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106152840-A-G

http://identifiers.org/hco/18/GRCh38#62780859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106152888-C-A

62781272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106153613-C-T

62781401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106154028-G-A

62781402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106154048-C-T

62781430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106154074-G-A

62781454-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106154098-C-G

62781823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106154393-A-G

62782144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106154699-C-T

62783055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106156057-A-G

62783508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106156581-G-A

62783508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106156581-G-C

62783513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106156586-C-G

62783702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106156874-T-C

62783800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106156974-C-T

62784345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106157513-C-T

62784933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106159438-A-G

62785846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160545-T-C

62786093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106160806-C-T

62786348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106161295-C-T

62786354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106161301-T-G

62787845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106162656-T-G

62788337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106165542-A-G

62788407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106165612-A-G

62789067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106166773-A-G

62789409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106167122-T-C

62789578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106167316-C-T

62789598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106167336-C-T

62790038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106167730-A-G

62790120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106167829-G-A

62790120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106167829-G-T

62790128-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106167837-T-A

62790926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106168875-C-T

62791225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106169167-A-T

62791350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106169256-T-C

62791375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106169281-C-G

62791375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106169281-C-T

62791507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106169385-G-A

62791649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106169525-G-T

62791892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106169747-T-A

62792113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106169984-T-G

62792382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106170255-T-C

62792563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106170430-A-G

62793523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106171469-C-T

62793818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106171683-G-A

62793948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106171799-A-G

62794089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106171898-G-C

62794326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106181761-C-T

62795880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106184522-G-A

62796178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106184783-T-G

62796624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106185196-G-A

62796973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106187618-T-G

62797373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188037-G-A

62797443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188162-A-T

62797595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188312-G-C

62797802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188450-G-A

http://identifiers.org/hco/18/GRCh38#62797994-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106188610-A-C

62798334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188855-A-G

62798334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188855-A-T

62798403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188923-C-T

62798416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106188936-C-T

62798677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106190397-G-A

62798682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106190403-T-C

62803205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106191118-T-C

62805860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106192094-A-T

62806579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106192926-T-C

62806645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106192976-G-A

62806763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106193090-G-A

62806896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106193227-C-T

62810103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106195162-A-G

62811224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106197830-A-G

62811225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106197831-T-A

62811430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106197993-G-A

http://identifiers.org/hco/18/GRCh38#62812402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#106198953-C-A

62812623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106199153-G-T

62812983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106199462-A-G

62813968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106200651-C-T

62814312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106200954-T-C

62814312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106200954-T-G

62814818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106201413-A-T

62814905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106201499-A-G

62826140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106204432-G-A

62826177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106204491-T-A

62826177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106204491-T-C

62826177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106204491-T-G

http://identifiers.org/hco/18/GRCh38#62826189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106204507-A-C

62826189-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106204507-A-T

http://identifiers.org/hco/18/GRCh38#62826236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106204553-C-A

62826236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106204553-C-T

62826245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106204562-G-A

62826245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106204562-G-T

62827272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106206229-T-A

62827272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106206229-T-C

62827446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106206405-T-C

62827882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106206828-T-C

62828090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106207069-T-C

62828740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106208026-G-T

62828741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106208027-G-A

62828741-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106208027-G-C

62828858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106208324-C-T

62829093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106208499-C-T

62830018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106209076-G-T

http://identifiers.org/hco/18/GRCh38#62830138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106209196-C-A

62830703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106209452-A-G

62830713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106209462-G-A

62830786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106209488-A-G

62830885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106209589-A-G

http://identifiers.org/hco/18/GRCh38#62830918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106209622-A-C

62831348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106210007-T-C

62832032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106210575-T-C

62832068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106210617-T-C

http://identifiers.org/hco/18/GRCh38#62832199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106210738-C-A

62832301-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106210852-A-T

62832876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106211382-G-T

62832883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106211389-C-T

62834536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106213157-C-T

62834583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106213185-T-C

62838502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106214457-G-A

62838502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 106214457-G-T

62838539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106214504-A-G

62838552-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106214517-A-T

http://identifiers.org/hco/18/GRCh38#62838666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106214631-C-A

62838666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106214631-C-G

62838666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106214631-C-T

http://identifiers.org/hco/18/GRCh38#62838766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106214703-C-A

http://identifiers.org/hco/18/GRCh38#62839018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106214911-C-A

62839018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106214911-C-T

62839142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106216402-T-A

62839220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106216480-A-G

62839327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106216583-T-G

62839830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106216709-G-T

62840278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106217132-A-G

62840278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106217132-A-T

62840434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106217270-A-G

62840498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106217324-T-G

62840602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106217414-C-T

62840673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106217481-A-G

62842723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106221239-T-C

62842986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106228582-C-T

62842996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106228590-G-T

62843059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106228629-C-T

62843219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106228747-A-G

62843416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106228929-T-C

62843639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106229078-A-G

62844929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106230471-G-A

62845282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106231082-A-G

http://identifiers.org/hco/18/GRCh38#62845579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106231321-A-C

62845625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106231356-C-T

62845663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106231394-A-G

62845832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106231545-G-A

62846646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106234172-T-C

62846649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106234175-A-G

62847043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106234523-G-A

62847068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106234535-T-C

62847070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106234537-G-A

62847093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106234557-C-T

62847153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106234607-T-C

62847487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106234900-G-A

62847913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106235420-G-A

62847913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106235420-G-T

62847920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106235427-A-G

62847960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106235466-T-C

62848073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106235567-A-T

62848232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106235723-G-T

62848913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106236091-G-T

62849050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106236221-A-G

62849067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106236235-A-G

62849187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106236334-A-G

62849259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106236412-A-G

62849259-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106236412-A-T

62849303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106236458-C-T

62849851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106236812-G-A

62849851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106236812-G-T

62849864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106236825-T-G

http://identifiers.org/hco/18/GRCh38#62849869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106236830-A-C

62850511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106237207-C-T

http://identifiers.org/hco/18/GRCh38#62850610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106237306-A-C

62850610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106237306-A-G

62850713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106237414-A-G

62850811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106237485-G-T

http://identifiers.org/hco/18/GRCh38#62850812-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#106237486-A-C

62850949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106237613-T-G

62852307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106241903-G-A

http://identifiers.org/hco/18/GRCh38#62852310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106241906-A-C

62852723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106242479-T-C

62852844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106242598-G-A

62853192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106242916-C-T

62853249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106242970-G-A

62853369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106243056-T-G

62854129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106243746-G-A

62854148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106243753-T-G

62854166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106243767-G-T

62854265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106243878-A-G

62854464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106244118-A-G

62854620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106244281-G-T

62855220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106244533-T-C

62855228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106244541-A-G

62855326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106244630-G-C

62855569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106244831-G-A

62855738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106244998-T-C

62855850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106245105-C-T

62855948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106245204-G-C

62858262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106245442-C-T

62860405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106246556-G-T

62860622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106246766-A-G

62860640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106246784-G-A

62860640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106246784-G-T

62860734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106246875-A-T

http://identifiers.org/hco/18/GRCh38#62860751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106246892-A-C

62860751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106246892-A-G

62861087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106247229-A-G

62861183-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106247348-C-G

62861195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106247360-C-T

62875313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106248872-A-G

62875502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106249141-T-G

62876063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106249354-G-C

62876166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106249467-T-A

62876207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106249519-A-G

62876349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106249844-G-A

62876364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106249860-C-G

62876472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106249952-T-C

62876704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106250259-C-T

62876997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106250529-C-T

62877470-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106250971-T-G

62877661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106251140-C-T

http://identifiers.org/hco/18/GRCh38#62877758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#106251234-C-A

62877758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106251234-C-T

62877921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106252026-A-G

62877957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106252058-A-G

http://identifiers.org/hco/18/GRCh38#62877958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106252059-A-C

62878015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106252118-A-G

62878136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106252241-C-T

62878334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106252428-C-G

62878334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106252428-C-T

62878339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106252433-T-G

http://identifiers.org/hco/18/GRCh38#62878440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106252519-A-C

62878440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106252519-A-G

http://identifiers.org/hco/18/GRCh38#62878674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106252713-C-A

62878674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106252713-C-T

62880164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106253022-C-T

62880174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106253028-T-C

62880415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106253241-G-A

62880415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106253241-G-C

62880639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106253438-A-G

62880673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106253467-A-G

62881412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106254166-A-G

62881582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106254375-G-T

62882040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106254809-C-T

62882217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106254948-G-A

62884667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106256415-A-G

62884775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106256641-A-T

62884776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106256642-T-G

62884851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106256725-G-A

62885020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106256896-A-G

62885101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106256960-A-G

62885292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106257124-G-A

62885868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106258677-A-G

62886623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106259057-C-G

62886623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106259057-C-T

62886677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106259109-A-G

62886735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106259162-G-A

62887047-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106259488-C-G

62887150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106259589-A-T

62887539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106260052-T-A

62894789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106266294-A-T

62894804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106266302-A-G

62894907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106266380-T-C

http://identifiers.org/hco/18/GRCh38#62895014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106266470-C-A

62895068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106266524-G-A

http://identifiers.org/hco/18/GRCh38#62895164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106266620-A-C

62895168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106266624-C-G

62895168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106266624-C-T

http://identifiers.org/hco/18/GRCh38#62895208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106266648-C-A

62895213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106266653-T-A

62895213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106266653-T-C

62895219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106266659-G-A

62895236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106266676-A-G

http://identifiers.org/hco/18/GRCh38#62895265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106266705-C-A

http://identifiers.org/hco/18/GRCh38#62895271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106266711-C-A

62895271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106266711-C-T

62895443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106266857-T-C

http://identifiers.org/hco/18/GRCh38#62895660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106267065-C-A

62895660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106267065-C-T

62895706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106267096-A-G

62895743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106267133-A-G

62895950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106267339-G-A

http://identifiers.org/hco/18/GRCh38#62896031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106267420-A-C

62896031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106267420-A-G

http://identifiers.org/hco/18/GRCh38#62896095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106267467-C-A

62896095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106267467-C-G

62897913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106268544-T-G

http://identifiers.org/hco/18/GRCh38#62898007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106268644-C-A

62898007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106268644-C-G

62898007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106268644-C-T

62898046-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106268669-T-A

62898067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106268690-T-G

http://identifiers.org/hco/18/GRCh38#62898075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106268693-C-A

62898075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106268693-C-T

62898099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106268715-G-T

62898193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106268804-G-T

62901201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106269841-T-C

62901415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106270041-C-G

62901415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106270041-C-T

62901468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106270093-G-A

62901468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106270093-G-C

62901486-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106270111-T-G

62902004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106270250-T-C

http://identifiers.org/hco/18/GRCh38#62902308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106270553-A-C

62902308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106270553-A-G

62902390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106270634-C-T

62902657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106270827-G-A

62902731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106270901-G-A

http://identifiers.org/hco/18/GRCh38#62902871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106271026-C-A

http://identifiers.org/hco/18/GRCh38#62902892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106271047-C-A

62902935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106271076-T-C

62903221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106271346-G-C

62903308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106271434-A-G

62904968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106272393-G-C

62905099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106272492-A-G

62905099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106272492-A-T

http://identifiers.org/hco/18/GRCh38#62905195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106272570-C-A

62905195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106272570-C-G

62905195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106272570-C-T

62905561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106272871-C-T

62905584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106272891-T-A

http://identifiers.org/hco/18/GRCh38#62905788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106272954-A-C

62905803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106272967-C-T

62912913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106273663-G-T

62913080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106273784-C-T

http://identifiers.org/hco/18/GRCh38#62913120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106273821-C-A

62913120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106273821-C-T

62913287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106273992-T-C

62914254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106274175-T-G

62914860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106274478-G-T

http://identifiers.org/hco/18/GRCh38#62914886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106274784-C-A

62914958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106274860-G-A

62915042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106274946-A-G

62915291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106275167-A-G

62915353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106275228-G-A

62915394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106275266-C-G

62915671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106275829-T-C

62916206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106276556-G-T

62916470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106276759-T-A

62916779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106277044-A-G

62916779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106277044-A-T

http://identifiers.org/hco/18/GRCh38#62916782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106277047-C-A

62916782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106277047-C-G

62916782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106277047-C-T

62917839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106277321-A-T

http://identifiers.org/hco/18/GRCh38#62918304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106277464-C-A

62918304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106277464-C-G

62918334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106277491-G-A

62918351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106277510-T-C

62918352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106277511-A-G

62919852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106278125-A-G

62919852-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106278125-A-T

62919894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106278166-G-A

62919894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106278166-G-C

http://identifiers.org/hco/18/GRCh38#62920040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106278343-C-A

62920198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106278508-T-C

http://identifiers.org/hco/18/GRCh38#62920218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106278519-C-A

62920218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106278519-C-T

http://identifiers.org/hco/18/GRCh38#62920254-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106278554-C-A

62920985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106279210-G-A

62921021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106279244-T-C

62923852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106279452-G-A

62923978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106279550-A-G

62924483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106280081-T-C

62924710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106280277-G-A

62924743-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106280317-T-G

62924831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106280393-C-T

62925777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106281251-T-C

62926381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106281784-C-G

62926511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106281890-G-A

62926727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106282103-G-A

62926727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106282103-G-T

62926757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106282131-C-T

http://identifiers.org/hco/18/GRCh38#62927719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106283109-A-C

62927772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106283163-A-G

62937125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106287262-T-A

62937155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106287290-A-G

http://identifiers.org/hco/18/GRCh38#62937434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106287529-A-C

62937656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106287737-A-G

62938287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106288006-A-G

62938305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106288024-G-A

62938615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106288301-C-G

62939360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106288749-G-A

62939533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106288847-A-T

62939551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106288861-G-A

62939551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106288861-G-T

62939623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106288928-C-G

62939660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106288974-A-G

62941028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291188-C-G

62941062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291228-G-A

http://identifiers.org/hco/18/GRCh38#62941555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106291800-A-C

http://identifiers.org/hco/18/GRCh38#62941625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106291868-C-A

62941665-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291909-T-A

62941665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291909-T-C

62941667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291911-G-C

62941667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291911-G-T

62941832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106292085-A-G

http://identifiers.org/hco/18/GRCh38#62941855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106292108-C-A

62941855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106292108-C-T

62941985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106292226-G-A

62942019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106292263-T-C

62942053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106292296-T-C

62942207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106292450-C-T

62942521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106294826-T-C

62942524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106294829-C-G

62942920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106295129-T-C

62942989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106295169-G-A

62943125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106295293-G-C

62943146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106295313-T-C

62943151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106295318-G-A

62943831-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106295644-A-T

http://identifiers.org/hco/18/GRCh38#62944132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106295924-C-A

62944132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106295924-C-T

62944590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106296282-A-G

62944672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106296350-A-G

62944993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106296631-T-C

62945006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106296644-G-A

62945208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106296843-C-G

62945208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106296843-C-T

http://identifiers.org/hco/18/GRCh38#62945305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106296937-A-C

62945305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106296937-A-G

62948486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106297719-C-T

62948490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106297723-G-A

62948490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106297723-G-C

http://identifiers.org/hco/18/GRCh38#62948738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106298128-A-C

62948966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106298342-T-C

62948993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106298372-T-C

62950033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106299315-C-G

62950033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106299315-C-T

http://identifiers.org/hco/18/GRCh38#62950246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106299511-C-A

62950605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106299809-G-T

62950677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106299871-C-T

62950678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106299872-G-A

62952280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106300664-G-A

62952347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106300732-C-T

62952428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106300834-C-T

62958240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106303577-G-C

62958346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106303687-G-A

62958347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106303688-C-T

62958515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106303821-A-G

62958555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106303837-G-T

62958594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106303870-C-G

62958594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106303870-C-T

62958606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106303880-G-T

62958697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106303959-G-A

62958785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106304044-C-G

62958810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106304069-G-A

62958810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106304069-G-T

62959107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106304350-G-A

62959310-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106304525-G-C

62959606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106304787-G-A

62959794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106304963-A-G

62959982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106305165-G-A

62960225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106305453-C-T

62960547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106305708-T-C

62961380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106307015-A-G

http://identifiers.org/hco/18/GRCh38#62961493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106307098-C-A

62963234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106307929-G-C

62963234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106307929-G-T

62963269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106307961-A-G

62963269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106307961-A-T

62963275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106307967-T-A

62963275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106307967-T-C

62963275-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106307967-T-G

62963290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106307975-T-C

62963290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106307975-T-G

http://identifiers.org/hco/18/GRCh38#62963296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106307981-C-A

62963296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106307981-C-G

62963296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106307981-C-T

62963321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106308006-A-G

62963321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106308006-A-T

62963323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106308008-A-G

62963335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106308020-T-C

http://identifiers.org/hco/18/GRCh38#62963352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106308029-C-A

62963352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106308029-C-G

62963352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106308029-C-T

62963361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 106308038-T-C

62963411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106308091-G-A

62963416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106308096-C-T

62963509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106308189-C-T

62963525-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106308200-T-G

62963546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106308218-T-C

62963568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106308249-T-A

62963568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106308249-T-G

http://identifiers.org/hco/18/GRCh38#62963569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106308250-C-A

62963650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106308323-G-A

62964209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106308845-G-C

62972164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106313260-G-A

62972265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106313353-T-A

62972501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106314044-G-A

62972597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106314140-T-C

62972731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106314273-A-G

http://identifiers.org/hco/18/GRCh38#62972767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106314368-C-A

http://identifiers.org/hco/18/GRCh38#62972791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106314414-C-A

62972791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106314414-C-T

62972807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106314431-A-G

62972817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106314436-A-G

http://identifiers.org/hco/18/GRCh38#62972935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106314529-A-C

62973032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106314617-T-C

62973110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106314700-C-T

62973127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106314716-C-T

62973184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106314752-A-G

62973278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106314846-A-T

http://identifiers.org/hco/18/GRCh38#62973281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106314849-A-C

62973315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106314883-G-A

62973468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106315032-A-G

62973594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106315157-G-C

62973967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106315474-C-G

http://identifiers.org/hco/18/GRCh38#62974250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106315694-C-A

62974378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106315817-T-C

62974471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106315904-C-T

62975063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106317109-G-A

62975114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106317160-G-A

62975637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106317644-G-A

62975651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106317654-G-A

62975651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106317654-G-C

62975667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106317669-G-A

62975667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106317669-G-T

http://identifiers.org/hco/18/GRCh38#62975676-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106317678-A-C

http://identifiers.org/hco/18/GRCh38#62975712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106317710-C-A

62975712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106317710-C-T

62975749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106317745-A-T

62975750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106317746-A-G

62975760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106317756-C-T

http://identifiers.org/hco/18/GRCh38#62975766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106317762-A-C

62975766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106317762-A-G

62975831-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106317854-T-A

62976086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106318043-A-G

62976117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106318058-C-T

62976169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106318100-A-G

62976169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106318100-A-T

62977162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106319003-G-A

62977321-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106319160-T-A

http://identifiers.org/hco/18/GRCh38#62977442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106319284-A-C

62977642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106319463-C-T

62977706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106319508-A-G

62978160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106319773-G-A

62978160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106319773-G-T

http://identifiers.org/hco/18/GRCh38#62978232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106319832-C-A

62978232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron variant
orthologous variants: 106319832-C-T

http://identifiers.org/hco/18/GRCh38#62978258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106319855-C-A

62978294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106319891-G-A

62978294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106319891-G-T

62978301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106319898-C-T

62978426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106320023-G-A

http://identifiers.org/hco/18/GRCh38#62978606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106320203-C-A

62978606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106320203-C-G

62978705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106320302-G-A

http://identifiers.org/hco/18/GRCh38#62978762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106320359-C-A

62978762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106320359-C-T

62978876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106320473-C-T

62978994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106320591-C-T

62978997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106320594-G-A

62979335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106320932-G-A

62979335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106320932-G-T

62979338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106320935-G-A

62979338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106320935-G-C

http://identifiers.org/hco/18/GRCh38#62979346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106320955-C-A

62979346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: missense variant
orthologous variants: 106320955-C-T

62979347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106320956-G-A

62979347-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106320956-G-T

http://identifiers.org/hco/18/GRCh38#62979353-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106320962-A-C

62979353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106320962-A-T

http://identifiers.org/hco/18/GRCh38#62979356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106320995-C-A

62979356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106320995-C-T

62979389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: synonymous variant
orthologous variants: 106321028-C-T

62979712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 3 prime UTR variant
orthologous variants: 106321344-T-C

62979712-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 3 prime UTR variant
orthologous variants: 106321344-T-G

http://identifiers.org/hco/18/GRCh38#62979733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106321365-A-C

62979733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 3 prime UTR variant
orthologous variants: 106321365-A-G

62979890-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 3 prime UTR variant
orthologous variants: 106321497-A-T

http://identifiers.org/hco/18/GRCh38#62980016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106321624-A-C

62980099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 3 prime UTR variant
orthologous variants: 106321697-T-C

http://identifiers.org/hco/18/GRCh38#62980229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106321801-C-A

62980294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 3 prime UTR variant
orthologous variants: 106321837-G-C

62980294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 3 prime UTR variant
orthologous variants: 106321837-G-T

62980303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 3 prime UTR variant
orthologous variants: 106321846-A-G

http://identifiers.org/hco/18/GRCh38#62980396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20610
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#106321938-C-A