96304455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41017837-C-T

96304468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41017850-G-A

96304474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41017856-C-T

http://identifiers.org/hco/10/GRCh38#96304497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41017877-C-A

96304554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 41017934-G-A

96304581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 41017961-A-T

http://identifiers.org/hco/10/GRCh38#96304731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41018109-A-C

96304751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41018128-G-T

96304969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41018276-A-T

96305001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41018308-T-C

96305008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41018314-C-T

96305098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41018402-G-A

96305117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41018421-T-C

96305174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41018468-C-G

96305194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41018486-G-A

96305343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41018611-G-C

96305371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41018634-G-A

96305376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41018639-G-T

96305436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41018678-G-A

96305493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41018729-C-T

96305860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41019073-A-T

96306053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41019252-G-T

96306398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41019308-A-G

http://identifiers.org/hco/10/GRCh38#96306468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#41019378-A-C

96306485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41019395-G-T

96306622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41019531-G-A

96306689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41019590-A-G

96306702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41019601-A-G

96306706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41019605-G-A

96306706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41019605-G-T

96306751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41019637-C-T

96306814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41019696-A-G

96306816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41019698-T-C

96306818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41019700-T-C

96307204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41020076-A-G

96307227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41020099-T-C

96307321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41020177-T-G

96307348-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41020204-T-G

96307355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41020231-T-G

http://identifiers.org/hco/10/GRCh38#96307379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41020255-C-A

96307379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41020255-C-G

96307379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41020255-C-T

http://identifiers.org/hco/10/GRCh38#96307382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41020258-A-C

96307382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41020258-A-G

96307382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41020258-A-T

96308385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41021450-G-A

http://identifiers.org/hco/10/GRCh38#96308413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41021478-A-C

96308413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41021478-A-G

96308452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41021516-G-A

96308533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41021610-C-G

96308533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41021610-C-T

96309561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41022677-C-G

96309565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41022681-C-T

96310964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41022794-T-C

96311125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41022929-A-G

96311339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41023118-A-G

96311397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41023160-A-G

96311477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41023244-G-A

96313972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41024528-C-G

96314241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41024773-A-G

96314350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41024906-T-G

96314814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025061-A-G

96314865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025115-A-G

96314885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025139-A-T

96314954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025204-G-A

96315054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025301-C-T

96315055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025302-G-A

http://identifiers.org/hco/10/GRCh38#96315102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41025346-C-A

http://identifiers.org/hco/10/GRCh38#96318262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41025498-C-A

96318263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025499-A-G

96318263-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025499-A-T

96318315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025551-G-T

96318316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025552-A-T

96318343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025579-A-G

96318443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: missense variant
orthologous variants: 41025678-C-G

96318443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: missense variant
orthologous variants: 41025678-C-T

http://identifiers.org/hco/10/GRCh38#96318475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41025710-A-C

96318475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: missense variant
orthologous variants: 41025710-A-T

96318582-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025798-G-C

http://identifiers.org/hco/10/GRCh38#96318599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41025816-C-A

96318599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025816-C-G

96318599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025816-C-T

96318604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025821-G-A

96318644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025841-G-T

96318667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025864-G-A

96318667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025864-G-T

96318677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025874-C-T

96318678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025875-T-A

http://identifiers.org/hco/10/GRCh38#96318681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41025878-C-A

96318700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41025891-G-A

96318767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41026093-T-C

96318775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41026101-C-T

96318893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41026272-C-T

96319135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41027149-A-G

http://identifiers.org/hco/10/GRCh38#96319166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41027179-C-A

96319166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41027179-C-T

http://identifiers.org/hco/10/GRCh38#96319245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41027296-C-A

96319245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41027296-C-T

96319276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: synonymous variant
orthologous variants: 41027327-T-C

96319342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: synonymous variant
orthologous variants: 41027393-T-C

96319342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: stop gained
orthologous variants: 41027393-T-G

96319396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41027447-G-A

96319396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41027447-G-T

http://identifiers.org/hco/10/GRCh38#96319438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41027487-C-A

http://identifiers.org/hco/10/GRCh38#96319445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41027494-C-A

96319484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41027532-C-G

96319967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41027615-C-G

96320123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41027758-C-T

96320277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41027912-C-T

96320556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41028166-G-A

96320556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41028166-G-C

96320556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41028166-G-T

96320692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: synonymous variant
orthologous variants: 41028287-A-G

http://identifiers.org/hco/10/GRCh38#96320837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41028426-C-A

96320837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41028426-C-T

96321832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41028501-C-T

96322064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41028717-C-T

96322111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41028766-C-T

96322112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41028767-G-A

96322165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, undefined
orthologous variants: 41028820-G-A

96322414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41029053-A-G

96322431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41029071-C-G

96322453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41029090-G-C

http://identifiers.org/hco/10/GRCh38#96322537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41029174-C-A

96322537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41029174-C-T

http://identifiers.org/hco/10/GRCh38#96322570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41029194-C-A

96322570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41029194-C-T

96322588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41029651-G-A

96322735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 41029798-G-T

96322781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41029846-A-G

96322790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41029855-G-A

96322790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41029855-G-T

96322819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41029879-A-G

96323301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41030242-A-G

http://identifiers.org/hco/10/GRCh38#96323600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41030372-A-C

96323921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41030842-G-A

96323921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41030842-G-T

96323962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41030959-G-A

http://identifiers.org/hco/10/GRCh38#96324114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41031152-C-A

96324114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031152-C-T

http://identifiers.org/hco/10/GRCh38#96324121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41031159-C-A

http://identifiers.org/hco/10/GRCh38#96324134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41031172-A-C

96324163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031201-G-T

96324222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031258-T-C

96324235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031271-G-A

http://identifiers.org/hco/10/GRCh38#96324237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41031273-C-A

96324237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031273-C-T

96324247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031283-G-A

http://identifiers.org/hco/10/GRCh38#96324248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41031284-C-A

96324248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031284-C-G

96324349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: synonymous variant
orthologous variants: 41031385-G-A

http://identifiers.org/hco/10/GRCh38#96324366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41031402-A-C

96324366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: missense variant
orthologous variants: 41031402-A-G

96324367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: synonymous variant
orthologous variants: 41031403-A-G

96324438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031472-G-A

96324438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031472-G-C

96324439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031473-T-G

96324454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031487-T-C

96324454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031487-T-G

http://identifiers.org/hco/10/GRCh38#96324461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41031494-C-A

96324461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031494-C-T

http://identifiers.org/hco/10/GRCh38#96324476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41031507-C-A

96324480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031511-G-T

http://identifiers.org/hco/10/GRCh38#96324485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41031516-C-A

96324485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031516-C-T

96324486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031517-T-C

96324581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031577-T-C

96324707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031675-C-T

96324757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031724-G-A

96324783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031744-G-A

96324868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031852-T-C

96324954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031929-G-A

96325005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41031987-C-T

96325053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41032030-G-A

http://identifiers.org/hco/10/GRCh38#96325127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41032121-A-C

96325127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41032121-A-G

96325265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41032935-G-T

96325494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41033167-T-A

96326167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41033311-C-T

96326942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41033985-A-G

96327426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41034597-C-G

96327441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41034612-C-T

96327463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 41034622-C-G

96327667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41034799-C-T

http://identifiers.org/hco/10/GRCh38#96327668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41034800-A-C

96327686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41034818-G-T

96327697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41034834-G-A

96327697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41034834-G-T

http://identifiers.org/hco/10/GRCh38#96327718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41034855-C-A

http://identifiers.org/hco/10/GRCh38#96327743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41034880-A-C

96327743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41034880-A-G

96327930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41035056-C-T

96328521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41035742-T-C

96328575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41035805-T-C

http://identifiers.org/hco/10/GRCh38#96328616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41035841-C-A

96328616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41035841-C-G

96328616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41035841-C-T

96328650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41035875-G-C

96328650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41035875-G-T

96328725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 41035968-G-A

96328746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: synonymous variant
orthologous variants: 41035989-T-C

96328746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: missense variant
orthologous variants: 41035989-T-G

http://identifiers.org/hco/10/GRCh38#96328764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41036007-C-A

96328785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: missense variant
orthologous variants: 41036028-T-G

96329004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41036259-G-C

96329096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41036369-T-G

96329252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41036713-C-T

96329253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41036714-G-A

96329371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41036884-G-T

96329499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41036987-C-T

96329610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41037089-A-G

96331015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41040818-A-G

96331021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41040824-G-T

96331026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41040829-G-A

http://identifiers.org/hco/10/GRCh38#96331071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41040873-A-C

http://identifiers.org/hco/10/GRCh38#96332059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41041190-C-A

96332214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41041301-A-G

http://identifiers.org/hco/10/GRCh38#96332240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41041319-C-A

96332240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41041319-C-T

96332578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: synonymous variant
orthologous variants: 41041661-G-A

http://identifiers.org/hco/10/GRCh38#96332687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41041733-A-C

96332687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41041733-A-G

96332688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41041734-G-T

96332691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41041737-G-T

96332698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41041744-G-A

96332698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41041744-G-T

96332733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41041784-T-A

96332733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41041784-T-C

96332745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41041796-G-A

96332745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41041796-G-T

http://identifiers.org/hco/10/GRCh38#96332747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41041798-C-A

96332921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41041960-T-G

96335282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41043642-G-C

96335553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41043865-A-G

96335590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41043904-G-A

96335591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41043905-C-T

96335596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41043910-G-A

96335678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41043981-C-T

96335753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41044051-G-C

96335753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41044051-G-T

96335768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41044066-G-A

96335768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41044066-G-T

http://identifiers.org/hco/10/GRCh38#96335790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41044087-A-C

96335816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41044127-T-C

http://identifiers.org/hco/10/GRCh38#96335817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41044128-A-C

96335817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41044128-A-G

96335834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41044145-T-C

96335841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41044152-G-A

96335857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41044168-T-C

96335917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: synonymous variant
orthologous variants: 41044225-T-C

96335926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: synonymous variant
orthologous variants: 41044234-T-C

96337076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41045403-T-G

96337492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41045813-T-C

96337636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41045951-A-G

96337637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: intron variant
orthologous variants: 41045952-G-T

96338357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: 3 prime UTR variant
orthologous variants: 41047715-A-G

96338407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: 3 prime UTR variant
orthologous variants: 41047792-T-C

96338408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: 3 prime UTR variant
orthologous variants: 41047793-A-G

http://identifiers.org/hco/10/GRCh38#96338493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41047888-C-A

96338493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: 3 prime UTR variant
orthologous variants: 41047888-C-T

http://identifiers.org/hco/10/GRCh38#96338540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2983
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#41047934-C-A