68053228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86671166-T-C

http://identifiers.org/hco/4/GRCh38#68053290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86671228-C-A

68053290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86671228-C-T

68053334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86671272-C-T

68053394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86671324-T-C

68053403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86671333-T-C

http://identifiers.org/hco/4/GRCh38#68053407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86671337-C-A

http://identifiers.org/hco/4/GRCh38#68053437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86671374-C-A

68053437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86671374-C-T

68053516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86671451-T-C

http://identifiers.org/hco/4/GRCh38#68053521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86671456-C-A

68053548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86671486-T-C

68053567-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86671505-T-G

68053595-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86671532-T-A

68053770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86671658-A-G

68053770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86671658-A-T

68053856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86671755-A-G

http://identifiers.org/hco/4/GRCh38#68053882-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86671845-A-C

68053956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 86671918-T-C

http://identifiers.org/hco/4/GRCh38#68054169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86672141-C-A

68054305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86672263-T-G

68054327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86672278-T-A

68054436-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86672400-C-G

68054532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86672497-C-T

68059129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86675889-T-G

68059278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86675973-C-T

68059304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86675997-T-C

68059307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86676000-G-T

68059317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86676010-T-C

http://identifiers.org/hco/4/GRCh38#68059362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86676055-A-C

68059362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 86676055-A-G

68059362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 3_prime_UTR_variant, intron_variant, stop_gained, undefined
orthologous variants: 86676055-A-T

68059749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86676277-T-C

68059777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86676305-C-T

68059811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86676330-C-T

http://identifiers.org/hco/4/GRCh38#68059894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86676395-C-A

68059945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86676445-G-C

68059978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86676478-G-A

68060066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86676560-G-C

68060082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86676575-T-C

http://identifiers.org/hco/4/GRCh38#68064731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86677796-A-C

68064731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 86677796-A-T

68064749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 86677814-T-C

68064899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 86677964-T-C

68064959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86678024-A-G

68064977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86678042-C-T

68065364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86678465-C-T

68065693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86678741-A-G

68067464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86680308-G-A

68067699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86680537-T-C

68067825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86680649-A-G

68067924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86680738-G-C

68068045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86680833-T-C

68068062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86680850-T-C

68068266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86681065-G-A

68068476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86681407-G-A

68068476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86681407-G-T

68068491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86681416-G-T

68068580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86681457-T-C

http://identifiers.org/hco/4/GRCh38#68068677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86681553-C-A

http://identifiers.org/hco/4/GRCh38#68068935-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86681761-C-A

68068935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86681761-C-G

68068935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86681761-C-T

http://identifiers.org/hco/4/GRCh38#68068939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86681765-C-A

68068939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86681765-C-T

68068940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86681766-A-G

http://identifiers.org/hco/4/GRCh38#68068950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86681776-C-A

68068950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86681776-C-T

68068959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86681806-T-C

http://identifiers.org/hco/4/GRCh38#68068961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86681808-C-A

68068961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86681808-C-T

68068969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86681816-G-T

68069320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86682519-G-T

68069326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86682525-A-G

68069490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86682670-G-A

68069497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86682680-C-T

68069530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86682714-C-T

68069560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86682729-G-A

68069652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86682786-A-T

68069939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86683037-A-G

68070030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86683120-T-C

http://identifiers.org/hco/4/GRCh38#68070081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86683171-C-A

68070081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86683171-C-T

68070086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86683176-A-G

68070108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86683198-G-C

68070108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86683198-G-T

68070332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86683401-G-A

68070512-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86683553-C-G

68070891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86684115-A-G

68070899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86684122-G-A

68071018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86684261-T-C

68071018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86684261-T-G

68071163-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86684372-A-T

68071224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86684426-G-A

68071268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86684462-G-T

68071639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86684741-A-G

68071994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685324-T-G

68072175-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685485-T-G

68072177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685487-A-G

68072193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685503-G-A

http://identifiers.org/hco/4/GRCh38#68072201-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86685546-A-C

68072201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685546-A-T

68072255-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685734-T-A

68072255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685734-T-C

68072255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685734-T-G

http://identifiers.org/hco/4/GRCh38#68072262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86685746-A-C

68072262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685746-A-G

68072262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685746-A-T

68072285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685810-G-A

68072285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685810-G-T

68072298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685823-T-A

68072298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685823-T-C

68072298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685823-T-G

68072308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685834-A-T

68072309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685835-A-G

68072309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685835-A-T

68072313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685839-A-G

68072320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86685846-T-C

68072346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 86685872-T-C

68072420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 86685946-A-G

68072486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_region_variant, synonymous_variant, undefined
orthologous variants: 86686012-A-G

68072494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 86686018-A-G

68072808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86686117-A-T

68073164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86686422-C-T

68073173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86686431-C-T

68073233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86686487-A-G

68073304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86686558-A-G

68073559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687171-G-A

68073578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687187-A-G

68073579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687188-C-T

68073629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687225-A-G

68073639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687235-C-T

68073640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687236-G-A

68073664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687260-T-C

http://identifiers.org/hco/4/GRCh38#68073894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86687506-C-A

68073897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687509-C-T

http://identifiers.org/hco/4/GRCh38#68073900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86687512-C-A

68073900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687512-C-T

68073907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687519-G-A

68073907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687519-G-T

68073959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 86687571-A-G

68074082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687644-T-A

68074082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687644-T-C

68074083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687645-A-G

68074083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687645-A-T

http://identifiers.org/hco/4/GRCh38#68074096-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86687658-A-C

68074096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86687658-A-G

68074476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86688523-A-T

68074540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86688587-T-C

http://identifiers.org/hco/4/GRCh38#68075182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86689015-C-A

68075344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 86689154-C-T

68075441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86689257-C-T

http://identifiers.org/hco/4/GRCh38#68075448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86689264-A-C

68075460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86689276-T-C

68075460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86689276-T-G

http://identifiers.org/hco/4/GRCh38#68075470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#86689286-C-A

68075470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86689286-C-T

68075665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86689994-T-G

68079735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86690172-T-G

68079874-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86690302-A-T

68080056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86690467-G-A

68080056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86690467-G-T

68080095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, undefined
orthologous variants: 86690506-T-C

68090625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: synonymous variant
orthologous variants: 86692740-A-G

http://identifiers.org/hco/4/GRCh38#68090631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86692746-A-C

68090631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: synonymous variant
orthologous variants: 86692746-A-G

http://identifiers.org/hco/4/GRCh38#68090716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86692808-C-A

68090716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86692808-C-T

http://identifiers.org/hco/4/GRCh38#68090719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86692811-C-A

68090719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86692811-C-T

http://identifiers.org/hco/4/GRCh38#68090787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86692865-A-C

68090787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86692865-A-G

68090787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86692865-A-T

68090850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86692926-A-G

http://identifiers.org/hco/4/GRCh38#68090859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86692935-C-A

68090908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86692979-A-G

68097228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86702810-C-T

http://identifiers.org/hco/4/GRCh38#68097293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86702865-C-A

68097293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86702865-C-T

68097403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86702959-C-T

68097433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86702982-T-C

68098674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86704562-T-C

68098747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86704635-C-T

68098757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86704645-T-C

http://identifiers.org/hco/4/GRCh38#68098765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86704653-C-A

68098765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86704653-C-T

http://identifiers.org/hco/4/GRCh38#68098808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86704694-C-A

http://identifiers.org/hco/4/GRCh38#68099046-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86704913-A-C

68099107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86704966-T-C

68099165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86705022-A-G

http://identifiers.org/hco/4/GRCh38#68100033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86707035-C-A

68100075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86707079-G-A

68100107-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86707112-A-T

68100112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86707146-A-T

68100384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86707416-G-A

68100747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86707723-T-C

68100880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86707852-C-T

68100920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86707888-G-C

68100920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86707888-G-T

http://identifiers.org/hco/4/GRCh38#68100994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86707961-C-A

68100994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86707961-C-T

68101151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86709521-T-A

68101323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86709683-G-A

68101425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86710250-G-A

68105903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86711558-A-G

68105947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86711598-A-T

68106091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86711738-C-G

68106156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86711796-C-T

68109110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86722608-T-C

http://identifiers.org/hco/4/GRCh38#68109188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86722682-C-A

68109189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86722683-C-T

http://identifiers.org/hco/4/GRCh38#68109276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86722746-A-C

68109478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86722898-G-A

68109807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86730408-T-C

68109847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86730450-G-A

68109847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86730450-G-T

68110044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86730645-A-G

68110089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86730690-T-A

68110089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86730690-T-G

68110292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86730900-A-G

68121306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86733436-G-A

http://identifiers.org/hco/4/GRCh38#68121322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86733452-A-C

68121438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86733541-C-T

68121947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86734104-A-G

68121980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86734137-A-G

68121981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86734138-C-T

68122033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86734170-T-A

http://identifiers.org/hco/4/GRCh38#68122176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86734318-A-C

68122470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86734610-C-T

68122779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86734895-T-C

68122999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86735090-A-G

68123134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86735247-T-C

68123664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86735781-G-C

68123854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86735934-T-C

http://identifiers.org/hco/4/GRCh38#68124976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86736569-C-A

68124976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86736569-C-T

68124990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86736577-A-G

68124990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86736577-A-T

68124997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86736584-A-T

68125186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86736742-T-C

68125505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86737041-T-C

68127940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86737655-G-A

68127969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86737684-T-G

68128054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86737773-A-G

68128054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86737773-A-T

68128938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86738492-C-T

68128959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86738513-G-A

http://identifiers.org/hco/4/GRCh38#68128977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#86738532-C-A

68129070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86738609-G-A

68129404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86738919-T-C

68129670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29994
most severe consequence: intron variant
orthologous variants: 86739131-T-C