64470264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 100634007-C-T

64470633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5 prime UTR variant
orthologous variants: 100634243-T-C

64470635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5 prime UTR variant
orthologous variants: 100634245-C-T

64470735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5 prime UTR variant
orthologous variants: 100634316-G-A

64470735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5 prime UTR variant
orthologous variants: 100634316-G-T

http://identifiers.org/hco/1/GRCh38#64470751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100634332-C-A

64470751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 100634332-C-G

64470751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 100634332-C-T

64470879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 100634502-G-A

64470879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 100634502-G-C

64470879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 100634502-G-T

64470974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100634587-G-A

64470974-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100634587-G-C

64470974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100634587-G-T

64471016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100634616-A-G

http://identifiers.org/hco/1/GRCh38#64471060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100634645-C-A

64471060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100634645-C-G

64471060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100634645-C-T

http://identifiers.org/hco/1/GRCh38#64471080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100634665-C-A

64471176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100634749-G-C

64471200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100634761-C-G

http://identifiers.org/hco/1/GRCh38#64471371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100634939-C-A

64471456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100635015-G-C

64471506-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100635061-C-G

64471506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100635061-C-T

64471812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100635320-G-A

64472479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100635857-A-G

http://identifiers.org/hco/1/GRCh38#64472547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100635925-C-A

64473067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100636402-G-A

64473067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100636402-G-T

64473086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100636421-C-T

64473195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100636531-C-T

64473261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100636599-A-T

64474219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100637496-A-G

64474232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100637509-A-G

64474470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100637734-G-A

http://identifiers.org/hco/1/GRCh38#64474985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100638459-C-A

64474985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100638459-C-T

64475089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100638557-T-C

64475101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100638569-T-C

http://identifiers.org/hco/1/GRCh38#64475941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100638842-C-A

64475941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100638842-C-T

64476167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100639036-C-T

64476223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100639091-A-G

64476306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100639176-G-A

64476473-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100639391-A-T

64476968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100639867-C-G

64477219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100640182-T-C

64477316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100640275-A-G

64477464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100640435-A-G

64477481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100640452-A-G

64477531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100640502-G-T

64477556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100640530-C-T

64478681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100641190-G-A

64478814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100641319-A-G

64478880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100641386-G-C

64478960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100641465-G-A

http://identifiers.org/hco/1/GRCh38#64479049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100641550-C-A

64479060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100641565-C-T

64479085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100641589-C-T

64479138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100641848-T-C

64479255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100641974-C-T

64479416-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100642115-G-C

64479432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100642131-A-G

64479491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100642168-A-G

64479588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100642260-T-C

64479589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100642261-T-A

64479638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100642309-C-T

64479643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100642314-C-T

64479831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100642479-A-G

64479926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100642576-C-G

64479962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100642611-C-T

64480173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100642753-A-G

64480290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100642864-G-A

64480344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100642904-C-G

64480469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100643017-A-G

64480476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100643024-T-G

64480779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100643862-A-G

64480801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100643870-T-C

64480878-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100643919-C-G

64480878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100643919-C-T

64480903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100643957-T-G

64481073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100644110-C-T

64481142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100644177-C-G

64481142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100644177-C-T

64482382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100645351-T-C

http://identifiers.org/hco/1/GRCh38#64482862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100645927-A-C

64482863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100645928-G-A

64482913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100645977-G-A

64482914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100645978-G-A

64482914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100645978-G-T

64482986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100646019-C-T

64483057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100646093-T-C

64483134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100646174-A-G

64486453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100647302-G-A

64486494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100647339-G-A

64486494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100647339-G-C

64486755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100647599-G-A

64487009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100647749-T-C

64487198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100647848-C-T

64487255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, undefined
orthologous variants: 100647902-A-G

64487541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100648306-A-G

64487588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100648351-T-C

64487604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100648368-G-C

64487747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100649100-G-C

64487872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100649214-C-G

64488123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100649464-A-G

64488199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100649559-G-A

64488221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100649581-T-C

64488251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100649607-A-G

64488453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100649795-G-T

http://identifiers.org/hco/1/GRCh38#64488875-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100650467-A-C

64489077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100650659-G-A

64489183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100650764-A-G

64489255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100650832-C-T

64489404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100650980-G-A

64489404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100650980-G-T

64489459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100651011-G-T

http://identifiers.org/hco/1/GRCh38#64490094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100652661-C-A

64490698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100653212-A-G

64491956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100653843-A-T

64492050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100653897-C-T

64492332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100654161-A-G

64492349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100654181-G-A

64492349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100654181-G-T

64492362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100654194-A-T

64492425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100654250-C-T

64492668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100654448-A-G

64492890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100654664-G-C

64492943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100654750-T-C

64492994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100654803-G-A

64493157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100654979-T-C

64493522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100655298-T-C

64493580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100655321-A-T

64493715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100655453-G-T

64493825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100655566-G-A

64494062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, undefined
orthologous variants: 100655809-T-C

64495024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100656689-C-T

64495135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100656801-C-T

64495470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100657120-T-C

64495497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100657146-C-G

64495753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100657383-G-A

64495945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100658388-G-T

64496268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100658684-T-C

64496494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100661460-C-G

64496643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100661617-A-G

http://identifiers.org/hco/1/GRCh38#64496705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100661677-A-C

64496810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100661775-C-T

http://identifiers.org/hco/1/GRCh38#64496833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100661799-C-A

64496939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100661870-G-C

64497196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100662163-C-T

http://identifiers.org/hco/1/GRCh38#64497253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100662283-A-C

64497264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100662294-T-C

64497640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100662655-C-T

64498782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100663266-A-G

64498782-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100663266-A-T

64498829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100663313-T-C

64499392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100664470-A-G

http://identifiers.org/hco/1/GRCh38#64501427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100667408-A-C

64501427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100667408-A-G

64501633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100667586-G-T

http://identifiers.org/hco/1/GRCh38#64502210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100667874-C-A

64502210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100667874-C-T

64502381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100668032-T-C

64502723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100668311-A-G

64502730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100668318-G-T

64502744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100668332-T-A

64502744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100668332-T-G

64502773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100668361-T-G

64503874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100669215-G-A

64504715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron variant
orthologous variants: 100669967-C-T

64507063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100672527-G-A

64507321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100672761-G-A

64507354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100672776-C-G

64507354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100672776-C-T

64507441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100672855-A-G

64507455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100672869-G-A

64507455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100672869-G-C

64508312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100674551-G-A

64508338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100674580-T-C

64508341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100674583-C-T

64508389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100674631-T-C

http://identifiers.org/hco/1/GRCh38#64508438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100674690-C-A

64508489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100674729-C-T

http://identifiers.org/hco/1/GRCh38#64508554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100674792-A-C

64508554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100674792-A-G

64508914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100675312-G-A

64508917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100675315-T-G

64509035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100675478-C-T

http://identifiers.org/hco/1/GRCh38#64509064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100675511-A-C

64509190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100675639-C-T

64509199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100675648-G-T

64509646-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100676100-C-G

64509852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100676293-G-A

64509862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100676303-T-G

http://identifiers.org/hco/1/GRCh38#64510481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100677397-A-C

64510514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100677425-T-C

64510852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100677717-C-G

64511232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100678061-G-A

http://identifiers.org/hco/1/GRCh38#64511328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100678159-A-C

64511352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100678181-T-G

64511681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100678416-C-T

64511682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100678417-G-A

64511699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100678425-T-A

64511699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100678425-T-C

http://identifiers.org/hco/1/GRCh38#64511737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100678457-C-A

64511760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100678480-G-T

64511780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100678502-G-A

http://identifiers.org/hco/1/GRCh38#64512422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100679147-A-C

64512554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100679249-A-G

64512591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100679268-C-T

64512641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100679318-A-G

64512812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100679487-C-T

64514201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100679865-G-T

64514537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100680187-G-A

64514566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100680202-A-G

64514600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100680235-T-C

64514645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100680279-T-C

64514689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100680324-G-A

64515292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100680992-T-C

64515420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100681117-G-A

64515755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100681433-G-C

64516093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100681848-G-A

64516200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100681917-T-C

64516200-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100681917-T-G

64516377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682525-C-T

64516457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682606-G-A

64516457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682606-G-C

64516556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682683-T-C

64516595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682722-T-C

64516624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682751-C-T

64516836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682951-T-G

64516894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100683011-G-A

64517269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100684181-C-G

64517333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100684243-C-T

64518012-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100684805-A-T

64518106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100684896-T-G

64518579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100685282-A-G

64518734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100685446-G-A

64518773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100685485-G-A

64518796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100685514-T-G

64519468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686215-T-C

64519695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686408-T-A

64519732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686500-G-A

64519732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686500-G-T

64519771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686572-T-C

64519773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686574-G-A

64519773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686574-G-T

64519827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686623-C-G

http://identifiers.org/hco/1/GRCh38#64519902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100686699-C-A

64519981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686785-G-A

64520230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100687035-A-G

64520492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100687300-T-G

64520659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100687471-G-C

64520880-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100687857-C-G

64520914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100687905-A-G

http://identifiers.org/hco/1/GRCh38#64521184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100688187-C-A

64521184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100688187-C-T

64525216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100697571-A-G

64525216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100697571-A-T

64525226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100697578-T-C

64525519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100697964-A-G

64525803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100698243-C-T

http://identifiers.org/hco/1/GRCh38#64525834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100698282-A-C

64526018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100698481-A-G

64526280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100698733-G-A

64526280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100698733-G-T

64526316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100698769-C-T

64526343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100698797-A-G

http://identifiers.org/hco/1/GRCh38#64526357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100698811-C-A

64526400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100698848-T-A

64526406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100698864-C-G

64526491-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100698972-T-A

64526528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100699009-C-G

64526707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100699162-G-A

64526817-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100699265-A-T

64527219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100699786-G-A

64527304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100699863-C-T

64527350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100699907-C-T

64527647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100700185-G-A

64527647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100700185-G-C

64527940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100700492-C-G

http://identifiers.org/hco/1/GRCh38#64528075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100700611-A-C

64528210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100700751-A-G

64528850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100701367-A-T

64529361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100701790-A-G

http://identifiers.org/hco/1/GRCh38#64529832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100702286-C-A

64529837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100702291-C-T

64529849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100702303-A-G

64530083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100702523-C-G

64531695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100703479-C-T

64531742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100703432-T-C

64535721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100703972-C-G

64535721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100703972-C-T

64535782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100704024-G-A

64535841-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100704077-T-G

64535842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100704078-G-A

64536104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100704317-A-G

64536235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100704652-A-T

64536652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100705055-G-A

64536777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100705174-T-C

64536946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100705322-G-C

64536975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100705351-A-G

64537068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100705435-C-T

64537095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100705479-G-A

64537155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100705538-C-T

64537231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100705657-T-C

64537242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100705723-A-G

64537424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100705899-T-G

64537696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100706185-T-C

64537736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100706221-G-C

64538927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100709381-T-C

64539103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100709551-T-C

64539511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100709968-T-C

64539605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100710030-T-G

64539719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100710137-C-T

64539754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100710173-A-G

64539869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100710305-G-A

64540064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100710554-G-A

64540064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100710554-G-C

64540064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100710554-G-T

64540178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100710655-A-G

64540339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100710788-T-C

64540429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100710873-T-C

64540990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100711427-G-A

64540990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100711427-G-C

64540993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100711430-T-C

64540996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100711433-G-A

64541307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100711753-A-T

http://identifiers.org/hco/1/GRCh38#64541414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100711861-A-C

64542148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100712620-T-C

64542190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100712661-G-A

64542253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100712731-G-A

64542268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100712763-G-T

64542379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100712867-C-T

64542427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100712913-C-T

64542519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100713036-G-A

64542570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100713109-G-A

64544089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100714566-C-G

64544089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100714566-C-T

http://identifiers.org/hco/1/GRCh38#64544913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100715368-C-A

64544913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100715368-C-T

64545054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100715523-G-T

64545086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100715557-C-T

64545194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100715627-G-C

64545205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100715638-G-A

64545213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100715646-G-T

64545219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100715652-A-T

64545241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100715670-A-G

64545241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100715670-A-T

64545357-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100715907-A-T

64545635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100716421-C-T

64545837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100716581-C-G

64546113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100716817-C-G

64546177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100716956-C-G

64546241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100717094-C-T

64546243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100717096-C-G

64546257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100717109-G-A

64546274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100717126-G-A

64546824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100717666-C-T

http://identifiers.org/hco/1/GRCh38#64546886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100717742-C-A

64546922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100717782-A-T

64547076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100717950-A-G

64548593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100719797-G-T

http://identifiers.org/hco/1/GRCh38#64548688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100719874-A-C

64548958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100720033-T-A

64548985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100720060-G-T

64549005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100720080-C-T

64549193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100720235-A-G

64549378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100721028-T-C

http://identifiers.org/hco/1/GRCh38#64549457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100721103-C-A

64549562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100721202-T-G

64549779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100721415-G-C

64549803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100721452-T-A

64549968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100721570-G-A

64550116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100721712-C-T

64550133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100721729-G-A

64550426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722023-G-A

64550449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722046-G-T

64550469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722067-A-T

64550486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722083-T-A

64550511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722106-T-C

http://identifiers.org/hco/1/GRCh38#64550591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100722176-C-A

64550687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722270-G-A

64550688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722271-T-A

64550688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722271-T-C

64550708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722291-G-A

64550708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722291-G-T

64550710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722293-G-A

64550710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722293-G-C

64550711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722294-G-A

64550742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722316-T-A

64550742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722316-T-C

http://identifiers.org/hco/1/GRCh38#64550760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100722335-C-A

64550760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722335-C-T

http://identifiers.org/hco/1/GRCh38#64550775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100722345-C-A

64550775-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722345-C-G

64551006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722540-C-T

64551178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722728-C-G

64551249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100722792-C-G

64551587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100723111-C-T

64551814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100723338-G-T

64552328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100723865-A-G

64552347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100723885-T-A

http://identifiers.org/hco/1/GRCh38#64553013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100724106-C-A

64553013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100724106-C-G

64553195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100724266-A-G

64553219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100724287-T-C

64553221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100724289-G-A

64553252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100724319-G-A

64553360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100724583-A-G

64553846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100725113-T-G

64554188-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100725568-T-G

64554190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100725570-T-A

64554307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100725705-A-G

64554456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100725843-T-C

64554557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100725980-G-A

64554569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100725992-G-T

64554580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100726003-G-A

64554593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100726019-C-T

http://identifiers.org/hco/1/GRCh38#64554610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100726036-A-C

64554628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100726057-G-A

64554628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100726057-G-C

64554741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100726184-A-G

64554819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100726267-T-C

64554915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100726355-G-A

64556130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100727265-G-T

64556184-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100727323-A-T

64556294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100727431-G-A

64556501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100727965-C-T

http://identifiers.org/hco/1/GRCh38#64556633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100728096-A-C

64556633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100728096-A-G

64556634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100728097-C-T

64556660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100728139-A-G

http://identifiers.org/hco/1/GRCh38#64556762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100728242-A-C

64556762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100728242-A-G

64557142-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100728364-T-A

64557298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100728526-T-C

http://identifiers.org/hco/1/GRCh38#64557357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100728578-A-C

64557377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100728598-A-G

64557424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100728649-C-T

64557577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100728774-G-A

64557610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100728806-C-T

64557650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100728848-C-G

64562975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100731802-G-C

64562999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100731836-G-A

64562999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100731836-G-T

http://identifiers.org/hco/1/GRCh38#64563132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100731924-A-C

64563283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100732022-T-A

64563335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100732066-C-T

64563344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100732075-A-G

64563371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100732102-T-A

64563543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100732236-A-G

64563626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100732315-T-A

http://identifiers.org/hco/1/GRCh38#64563627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100732316-C-A

http://identifiers.org/hco/1/GRCh38#64563628-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100732317-A-C

64563771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100732436-A-G

64563813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100732472-G-T

64563840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100732497-A-G

64563936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100732595-G-A

64563958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100732610-G-T

64564806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100732816-T-C

64566953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100734818-G-A

64567169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100735023-T-C

64567420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100735214-C-T

64567422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100735216-T-C

64567472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100735254-A-G

http://identifiers.org/hco/1/GRCh38#64567819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100736639-A-C

64567819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100736639-A-G

64567877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100736697-C-T

64567915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100736735-T-A

64567916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100736736-G-A

64567932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100736752-G-A

64567932-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100736752-G-C

64568151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100736967-G-A

64568642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100737410-A-T

64568847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100737603-A-G

64568877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100737633-C-T

64569441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100737997-G-T

http://identifiers.org/hco/1/GRCh38#64569495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100738050-C-A

64569509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100738063-G-A

64569579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100738138-G-A

64569861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100738345-C-G

64569992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100738457-C-T

64570057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100738545-T-A

http://identifiers.org/hco/1/GRCh38#64570228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100738788-C-A

64570228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100738788-C-T

64570245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100738805-A-G

64570322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100738883-A-G

64570322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100738883-A-T

64570338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100738899-A-G

http://identifiers.org/hco/1/GRCh38#64570464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100739028-C-A

64570563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100739119-C-T

64570588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100739159-G-T

http://identifiers.org/hco/1/GRCh38#64570638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100739205-C-A

64570688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100739254-G-A

64571593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: -A-G

64572521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100743527-A-G

64572907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100743886-T-C

64572952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100743931-G-A

http://identifiers.org/hco/1/GRCh38#64573140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100744708-C-A

64573255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100744815-C-T

64573277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100744824-C-G

64573277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100744824-C-T

http://identifiers.org/hco/1/GRCh38#64573811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100745238-A-C

64573811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100745238-A-G

64574247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100745658-C-T

64574248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100745659-G-A

64574432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100745819-C-G

64574773-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100746139-G-C

64574939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100746621-G-A

64574977-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100746654-G-C

64574977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100746654-G-T

64575054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100746731-A-G

64575056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100746733-A-G

64575194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100746860-A-G

64575411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100747056-A-G

64575547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100747201-G-A

64576049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100747701-T-C

64576156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100747809-G-A

64576494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100748152-G-A

64576586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100748225-C-T

64577947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100751101-G-A

64578300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100751440-G-A

64578329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100751470-T-C

http://identifiers.org/hco/1/GRCh38#64578401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100751533-C-A

http://identifiers.org/hco/1/GRCh38#64578444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100751578-C-A

64579160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100752513-A-G

http://identifiers.org/hco/1/GRCh38#64579267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100752610-A-C

64579535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100752863-G-A

64579536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100752864-G-T

64579592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100752919-T-C

64579592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100752919-T-G

64581280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100753980-G-A

64581683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100754394-T-C

64581831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100754526-T-C

64582006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100754721-A-G

64582006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100754721-A-T

64582007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100754722-C-T

64582029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100754743-G-A

64582029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100754743-G-T

64582290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100754988-A-T

64582385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100755079-G-T

64584455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100755182-C-T

http://identifiers.org/hco/1/GRCh38#64584631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100755302-A-C

64584631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100755302-A-G

64584693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100755372-C-T

http://identifiers.org/hco/1/GRCh38#64584701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100755380-A-C

64585085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100755679-T-G

http://identifiers.org/hco/1/GRCh38#64585141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100755735-A-C

64585172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100755758-T-C

http://identifiers.org/hco/1/GRCh38#64585259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100755823-A-C

64585269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100755836-G-C

64585332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100755891-G-A

64585423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100755975-T-C

64585479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100756029-G-A

64585527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100756092-C-T

64586939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100757385-C-T

64586961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100757404-A-G

64587065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100757508-C-G

64587435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100758390-A-G

64587559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100758517-G-A

64587874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100758897-T-A

64588093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759144-C-G

64588242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759268-A-G

64588265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759291-T-C

64588282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759308-C-T

64588757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759508-C-T

64588941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759678-A-G

64588957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759694-T-C

64589052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759761-C-T

64589090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759809-A-G

64589310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760021-A-T

64589553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760253-A-G

64589719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760423-A-T

64590384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100761048-C-T

64590514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100761165-T-C

64590584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100761228-C-T

64590588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100761232-G-A

64590623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100761267-A-G

http://identifiers.org/hco/1/GRCh38#64590717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100761396-A-C

64590717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100761396-A-G

64590851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100761554-G-C

64590996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100761784-T-G

64591093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762041-T-C

64591273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762176-C-G

64591273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762176-C-T

64591900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100762727-G-A

64592279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100763012-T-C

64592779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100763453-G-A

64592779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100763453-G-T

64592834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100763507-T-C

64592842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100763535-C-T

64593001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100764069-T-C

64593198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100764276-C-T

64593393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100764530-T-C

64593540-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100764658-G-C

64593603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100764712-G-A

64593627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100764735-T-C

64593633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100764741-A-G

64593815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100764918-A-T

64593919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100764988-G-A

64594565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100765527-C-T

64594580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100765542-C-T

64594611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100765593-T-C

64595024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100766026-A-G

64595207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100766205-G-A

64595228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100766211-G-T

64595238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100766221-C-T

64595288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100766261-G-A

64595470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100766444-G-A

64595590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100766527-A-G

64595651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100766590-G-A

64595926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100766837-G-T

64596370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100767278-G-A

64596391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100767299-T-C

64596638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100767512-C-T

http://identifiers.org/hco/1/GRCh38#64596738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100767625-C-A

64597184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100768083-A-G

64597297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100768196-G-A

64597311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100768210-G-A

http://identifiers.org/hco/1/GRCh38#64597509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#100768409-A-C

64597509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100768409-A-T

64597576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100768458-G-A

64597601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100768483-A-G

http://identifiers.org/hco/1/GRCh38#64597651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100768558-C-A

64597651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100768558-C-T

64597662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100768569-G-A

http://identifiers.org/hco/1/GRCh38#64597854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100768748-A-C

http://identifiers.org/hco/1/GRCh38#64598039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100768931-C-A

64598039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100768931-C-T

64598270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100769229-C-T

64598281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100769246-G-A

64598348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100769313-C-T

64598354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100769319-G-A

64598844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100769697-C-T

64599037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100769785-G-T

64599042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100769790-C-G

64599522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100770117-G-A

64599764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100770358-C-G

64599863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100770435-G-A

64600039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100770622-T-C

64600126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100770710-G-C

64600204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100770778-G-A

64600237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100770843-G-T

64600485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100771076-C-T

http://identifiers.org/hco/1/GRCh38#64600507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100771087-C-A

64602045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100774450-C-G

64602267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100774734-A-G

64602390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100774847-T-G

64602701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775124-A-G

64602701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775124-A-T

64602869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100775302-T-A

64602911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 100775344-A-G

64603080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775505-G-A

64603080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775505-G-T

64603407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775538-A-G

64603407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775538-A-T

64603433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775555-A-G

64603541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775664-G-A

64603590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775714-A-G

64603711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775834-G-A

64603778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775899-T-G

64603836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775958-A-T

64603878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100776006-G-A

64603888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100776016-T-C

64603936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100776064-A-T

64604362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100776501-A-T

64604614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100776715-A-G

http://identifiers.org/hco/1/GRCh38#64605682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100777750-C-A

64605682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100777750-C-T

64606058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100778153-A-G

64606258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100778515-G-T

64606367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100778617-T-C

64606379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100778629-A-G

64606410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100778651-G-C

64606412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100778653-A-G

64606492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100778740-G-A

64606492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100778740-G-T

64606523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100778771-A-G

64606552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100778799-G-C

64606845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100778874-G-C

64607573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100779465-A-G

64608062-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100780347-C-G

64608205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100780490-G-A

64608484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100780771-C-T

64608773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100781034-C-T

64608960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100781221-A-T

64608985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100781246-C-T

64608986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100781247-G-A

64608986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100781247-G-T

64609040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100781301-G-A

64609040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100781301-G-T

64618542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100783728-C-T

64618730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100783896-T-C

64618862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100784018-A-G

64618893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100784049-G-A

64618893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100784049-G-C

64618936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100784091-G-A

64619022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100784175-C-G

64619635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100785079-C-T

64619758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100785132-T-A

64619803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100785175-A-G

64619843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100785207-C-T

64620190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100785481-G-C

64620197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100785488-C-T

64621526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100796476-A-G

64621526-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100796476-A-T

64621690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100796631-G-A

64622133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100797032-G-A

64622987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100800167-A-G

64623064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100800244-C-G

64623490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100800366-A-G

64623525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100800390-G-T

64623857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100800891-C-T

64623919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100800947-T-A

64623986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801000-C-T

64624117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801136-T-C

64624117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801136-T-G

http://identifiers.org/hco/1/GRCh38#64624138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100801157-C-A

64624142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801161-C-G

64624288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801299-T-C

64624310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801321-C-T

64624340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801351-C-G

64624468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801480-G-C

64624871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100801906-T-C

64625166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100802200-G-A

64625166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100802200-G-C

64625966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100802373-A-G

64625972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100802379-G-A

64625972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100802379-G-T

64626096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100802492-A-G

64626165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100802553-A-G

64626174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100802561-A-G

64626195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100802577-A-T

64626703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100803213-C-T

64627598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100803731-A-G

64627632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100803763-A-G

64627689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100803823-G-A

64627724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100803858-G-A

64627879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100804002-T-C

64628107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100804502-G-T

64628126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100804513-G-A

64628241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100804619-C-T

64628307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100804680-A-T

http://identifiers.org/hco/1/GRCh38#64628385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100804758-C-A

64628430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100804804-G-A

64628527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100805470-G-A

64628576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100805514-G-A

64628829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100805743-A-G

64629094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100806000-C-G

64629121-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100806029-G-T

http://identifiers.org/hco/1/GRCh38#64629301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100806217-C-A

64629301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100806217-C-T

64629467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100806382-C-T

64629513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100806427-T-C

64629513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100806427-T-G

64629514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100806428-A-G

64629553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100806485-A-G

64629832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100806794-T-G

64630022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100806967-G-A

64630255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100807171-A-G

64630910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100807718-T-C

http://identifiers.org/hco/1/GRCh38#64631097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100807897-C-A

64631097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100807897-C-T

64631203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100808050-A-G

64631374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100808221-A-G

64631497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100808327-C-T

64631507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100808337-G-A

64631521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100808358-G-A

http://identifiers.org/hco/1/GRCh38#64631588-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100808421-A-C

64631666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100808495-T-C

64631768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100808583-C-T

64631801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100808613-G-T

64631867-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100808679-G-C

64631993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100808808-G-A

64632022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100808837-G-A

64632335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809004-T-C

64632368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809013-T-C

64632407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809028-C-T

64632475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809077-T-C

64632475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809077-T-G

http://identifiers.org/hco/1/GRCh38#64632507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100809112-C-A

64632507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809112-C-T

64632524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809164-G-T

64632526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809166-G-A

64632526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809166-G-C

64632526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809166-G-T

64632668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 100809272-A-G

64632674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 100809278-A-G

64632731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 100809335-T-C

64632823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809424-A-G

http://identifiers.org/hco/1/GRCh38#64633985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100810171-A-C

64634015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100810210-G-A

64634015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100810210-G-T

http://identifiers.org/hco/1/GRCh38#64634244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100810431-C-A

64634244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100810431-C-T

64635050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100810552-G-A

64635050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100810552-G-T

64635191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100810678-G-A

64635237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100810723-C-G

64635296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100810781-T-C

64637194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100812003-A-T

64637609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100812364-A-G

64637697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100812452-G-A

64637697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100812452-G-T

64637826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100812582-C-T

64638758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100813262-G-T

64638783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100813287-C-T

64639234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100814584-T-C

64639422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100814760-G-A

64639488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100814826-A-T

64639639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100814949-G-A

64639657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100814963-C-T

64639750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100815052-G-T

http://identifiers.org/hco/1/GRCh38#64640736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100815470-C-A

64640736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100815470-C-T

64641083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100815927-T-G

64641208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816047-G-C

64641559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816387-G-T

64641562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816390-T-C

64641601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816429-C-G

64641620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816441-G-T

64641681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816506-G-A

64641681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816506-G-C

64641681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816506-G-T

64641690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816515-A-G

64641748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816575-T-G

64641786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816613-A-G

64641797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816624-T-C

64641857-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100816684-T-A

64641857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100816684-T-G

64642036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816857-G-A

64642085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100816908-G-A

64642402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100817204-T-C

64642436-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100817224-G-C

64642448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100817236-T-C

64642533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100817318-C-T

64642534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100817319-G-A

64642553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100817334-G-T

64642644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100817402-T-C

64643896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100818404-G-A

64643952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100818481-C-G

64643952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100818481-C-T

64644328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100818806-A-G

64644656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100819073-C-G

64644656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100819073-C-T

64644669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100819086-C-T

64644707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100819102-T-C

64645990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100819929-G-T

64646099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100820001-A-G

64646284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100820163-T-C

64646371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100820245-C-T

64646386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100820260-G-A

64646386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100820260-G-T

64646525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100820386-C-T

64646850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100820570-T-C

64647042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100820751-T-A

64647149-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100820856-T-A

64647558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100821231-T-A

64647601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100821273-T-C

http://identifiers.org/hco/1/GRCh38#64647681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100821342-C-A

64647681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100821342-C-T

http://identifiers.org/hco/1/GRCh38#64647719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100821555-C-A

64647719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100821555-C-T

64647722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100821558-A-G

64647722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100821558-A-T

http://identifiers.org/hco/1/GRCh38#64647760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100821596-C-A

64647832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100821654-T-C

64647862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100821684-G-C

64647899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100821721-A-T

64647991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100821813-T-C

http://identifiers.org/hco/1/GRCh38#64648077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100821905-C-A

64648110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100821935-A-G

64648110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100821935-A-T

64651324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100822591-G-C

64651333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100822600-G-A

64651372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100822639-C-T

64651506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100822729-T-C

64652065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100823292-T-C

http://identifiers.org/hco/1/GRCh38#64652079-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100823306-A-C

64652079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100823306-A-G

64652372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100823598-A-G

http://identifiers.org/hco/1/GRCh38#64652382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100823615-C-A

64652455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100823688-T-A

64652519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100823745-C-T

64653595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100823971-A-G

64653597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100823973-G-A

64653612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100823988-G-T

64653631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100824006-G-A

64653631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100824006-G-C

64653642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100824016-G-C

64653642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100824016-G-T

64653656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100824030-G-A

64653774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100824159-C-T

http://identifiers.org/hco/1/GRCh38#64653947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100824329-C-A

64653947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100824329-C-G

64653947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100824329-C-T

64654126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100824727-A-G

64654302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100824872-A-G

64654306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100824876-A-G

64654309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100824879-G-A

64654309-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100824879-G-T

http://identifiers.org/hco/1/GRCh38#64654439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100825008-C-A

http://identifiers.org/hco/1/GRCh38#64654544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100825112-C-A

64654544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100825112-C-G

64654573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100825142-T-C

64654573-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100825142-T-G

64654588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100825157-A-G

http://identifiers.org/hco/1/GRCh38#64654623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100825191-C-A

http://identifiers.org/hco/1/GRCh38#64654632-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100825200-A-C

64654632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100825200-A-T

64654650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100825218-T-C

64654650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100825218-T-G

http://identifiers.org/hco/1/GRCh38#64654681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100825249-C-A

64654681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100825249-C-T

64654716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100825284-C-G

64654800-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100825368-G-C

64654800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100825368-G-T

64654814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100825382-G-A

http://identifiers.org/hco/1/GRCh38#64654840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100825408-C-A

64654914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100825462-A-G

64655560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100826383-G-C

http://identifiers.org/hco/1/GRCh38#64658566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100827975-C-A

64658566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100827975-C-T

http://identifiers.org/hco/1/GRCh38#64658570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100827979-C-A

64658570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100827979-C-T

64658791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100828164-C-T

http://identifiers.org/hco/1/GRCh38#64658953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100828356-C-A

64658953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100828356-C-G

http://identifiers.org/hco/1/GRCh38#64658954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100828357-C-A

http://identifiers.org/hco/1/GRCh38#64659651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100829277-A-C

64659739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100829373-C-G

64659831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100829454-G-A

64659867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100829489-C-T

64659928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100829547-G-A

64659991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100829610-C-G

64659991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100829610-C-T

http://identifiers.org/hco/1/GRCh38#64660060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100829686-C-A

64662801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100830567-A-T

64662891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100830653-T-C

64663643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100831150-A-G

64663720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100831228-T-A

64663810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100831318-C-G

http://identifiers.org/hco/1/GRCh38#64663985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100831503-C-A

64663985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100831503-C-T

http://identifiers.org/hco/1/GRCh38#64664119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100831631-C-A

64664119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100831631-C-T

64664222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100831714-A-G

64664286-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100831761-T-C

http://identifiers.org/hco/1/GRCh38#64664289-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100831764-A-C

64664289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100831764-A-G

64664295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100831770-G-T

64664408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100831880-G-A

64664408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100831880-G-T

http://identifiers.org/hco/1/GRCh38#64664409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100831881-C-A

64664409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100831881-C-G

http://identifiers.org/hco/1/GRCh38#64664435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100831908-C-A

64664443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 100831916-T-A

http://identifiers.org/hco/1/GRCh38#64664748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100832221-C-A

64664748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100832221-C-T

64664812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100832274-G-T

64664862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100832313-A-G

64664910-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100832364-T-A

64665021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100832471-C-T

64665639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100833434-A-G

64666039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100833524-T-C

http://identifiers.org/hco/1/GRCh38#64666150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100833636-C-A

64666189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100833675-T-C

64666847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100834165-T-A

64666847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100834165-T-C

64666872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100834261-A-G

64666886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100834276-G-A

64666886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100834276-G-T

64666923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100834300-G-A

64667174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100834533-T-C

64667538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100834880-A-G

64667573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100834916-T-C

http://identifiers.org/hco/1/GRCh38#64667589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100834923-C-A

64667632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100834966-T-C

64667713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100835039-T-A

64667739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100835065-G-A

64667999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100835252-T-G

64668726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100835455-C-T

64668748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100835477-G-A

64669078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100835809-A-G

64669567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100836137-C-T

64669677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100836228-A-G

64669749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100836291-G-A

64669801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100836329-G-A

64669844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100836359-A-G

64669910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100836418-A-G

64669919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100836427-G-T

64669963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100836488-T-C

64670012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100836538-A-G

64670153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100836657-C-T

64670407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100836925-G-A

64670792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100837244-T-C

http://identifiers.org/hco/1/GRCh38#64670839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100837291-A-C

64670841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100837293-C-G

64670841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100837293-C-T

64671138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100837581-G-C

64671234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100837756-G-A

64671311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100837986-A-G

64671423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100838081-G-A

64671423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100838081-G-T

64671440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100838093-G-A

64671440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100838093-G-T

64671464-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100838109-A-G

64671554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100838158-T-G

64671760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100838365-G-A

http://identifiers.org/hco/1/GRCh38#64671780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100838376-C-A

64671785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100838381-A-G

64671786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100838382-T-C

64671797-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100838392-T-A

64671808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100838403-G-T

64672146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100839580-A-T

64672239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100839672-G-A

64672346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100839781-A-G

64673054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100840414-A-T

64673093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100840449-T-C

64673113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100840458-A-T

64673264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100840608-G-A

64673455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100840798-C-T

64673510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100840837-A-G

64673599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100840890-A-G

64673612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100840903-C-T

64673685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100840975-G-A

64673755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100841773-G-T

64673889-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100841896-A-T

64674299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100842644-T-C

64674333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100842669-A-G

64674410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100842728-A-G

64674691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100843810-G-A

64674691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100843810-G-T

http://identifiers.org/hco/1/GRCh38#64674759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100843880-A-C

64674759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100843880-A-G

64674784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100843905-A-G

64675350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100845242-T-C

http://identifiers.org/hco/1/GRCh38#64675472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100845350-C-A

64675472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100845350-C-T

64675475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100845353-G-A

64675475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100845353-G-C

64675493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100845371-C-T

http://identifiers.org/hco/1/GRCh38#64675748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100845596-C-A

64675748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100845596-C-T

64675774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100845622-T-C

64675790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100845638-A-G

64675790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100845638-A-T

64675865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100845718-T-C

64676219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100846127-T-C

64676230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100846135-A-G

64676681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100846346-A-G

64676761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100846440-G-A

64676761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100846440-G-T

http://identifiers.org/hco/1/GRCh38#64676765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100846444-C-A

64676765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100846444-C-G

http://identifiers.org/hco/1/GRCh38#64676772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100846449-A-C

64676794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100846481-G-A

64676794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100846481-G-T

64676824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100846510-T-C

64676855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100846536-G-A

http://identifiers.org/hco/1/GRCh38#64676887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100846568-C-A

64676889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100846570-G-A

64676889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100846570-G-T

64676934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100846615-C-T

64677026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100846906-G-C

64677051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100846960-A-G

64677103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847009-A-G

64677135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847046-C-G

http://identifiers.org/hco/1/GRCh38#64677153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100847061-C-A

64677153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847061-C-T

64677159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847067-C-T

http://identifiers.org/hco/1/GRCh38#64677160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100847068-A-C

http://identifiers.org/hco/1/GRCh38#64677168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100847076-C-A

64677304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847196-G-A

64677501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847385-G-T

http://identifiers.org/hco/1/GRCh38#64677580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100847456-C-A

64677580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847456-C-T

64677581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847457-G-A

64677990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847866-C-T

64678043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847918-A-G

64678043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847918-A-T

64678049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847924-A-G

64678049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847924-A-T

http://identifiers.org/hco/1/GRCh38#64678081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100847954-C-A

http://identifiers.org/hco/1/GRCh38#64678091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100847964-C-A

64678091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847964-C-T

http://identifiers.org/hco/1/GRCh38#64678092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100847965-C-A

64678092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100847965-C-T

http://identifiers.org/hco/1/GRCh38#64678394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100848255-C-A

64678394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100848255-C-T

64678401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100848262-A-T

64678403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100848264-T-C

64678422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100848284-G-A

64678428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100848290-T-C

64678940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100848781-G-A

64679027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100849406-G-A

http://identifiers.org/hco/1/GRCh38#64679094-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100849470-A-C

64679172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100849535-C-T

64679264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100849614-G-A

64679421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100849756-C-T

http://identifiers.org/hco/1/GRCh38#64679437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100849772-C-A

http://identifiers.org/hco/1/GRCh38#64679467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100849799-C-A

64679467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100849799-C-G

64679469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100849801-A-G

http://identifiers.org/hco/1/GRCh38#64679474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100849806-A-C

64679474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100849806-A-T

64679635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100849966-T-C

64679814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100850125-G-A

64679814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100850125-G-T

64679972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100850263-C-T

64680137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100850418-T-G

64680631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100850551-C-T

64680770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100850673-C-G

64680870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100850741-C-T

64681154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100851128-G-A

64681154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100851128-G-T

64681182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100851156-G-A

64681182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100851156-G-C

http://identifiers.org/hco/1/GRCh38#64681187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100851161-C-A

64681505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100851463-G-A

64681505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100851463-G-T

64681549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100851496-T-G

64681550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100851497-T-G

http://identifiers.org/hco/1/GRCh38#64681594-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100851538-A-C

64681594-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100851538-A-T

64681880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100851804-G-T

64681895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100851819-T-C

64682001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 100851928-A-G

64682123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100852050-T-G

64682801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100853122-C-G

64683051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100853317-C-T

64683112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100853377-G-A

64683401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100853683-A-G

64683581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100853821-T-A

64683669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100853906-T-G

http://identifiers.org/hco/1/GRCh38#64683864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100854102-A-C

64683895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854135-C-T

64683928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854170-T-G

64685691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854359-A-T

64685737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854402-C-T

64685858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854520-G-A

64685911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854575-G-A

http://identifiers.org/hco/1/GRCh38#64685917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100854581-C-A

64685917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854581-C-T

64685919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854583-C-T

64685930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854594-G-A

64685942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854597-A-G

64686063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854713-A-G

64686192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854791-G-A

64686195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854794-T-C

64686232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100854832-G-T

64686532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100855090-C-T

64686648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100855203-A-G

64686649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100855204-T-C

64686836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100855431-A-T

64687202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100855744-A-G

64687202-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100855744-A-T

64687976-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100857349-C-G

64687996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100857367-A-G

64688196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100857539-C-T

64688503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100857792-A-G

64688592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100857891-C-T

64688650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100857939-C-T

64689728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100858744-A-G

64689844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100858837-T-G

http://identifiers.org/hco/1/GRCh38#64689861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100858854-C-A

64689906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100858896-A-G

64689967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100858941-C-T

64690122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100859076-A-G

64690279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100859243-T-A

http://identifiers.org/hco/1/GRCh38#64691113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100859868-A-C

64691167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100859926-A-G

http://identifiers.org/hco/1/GRCh38#64691211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100859970-C-A

64691211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100859970-C-T

http://identifiers.org/hco/1/GRCh38#64691212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100859971-C-A

64691212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100859971-C-T

64691223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100859982-A-G

64691232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100859991-A-G

64691354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100860090-T-C

64691381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100860117-C-G

64691399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100860135-T-C

64691399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100860135-T-G

64691400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100860136-G-A

64691501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100860237-T-G

http://identifiers.org/hco/1/GRCh38#64691563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100860299-A-C

64691563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100860299-A-G

http://identifiers.org/hco/1/GRCh38#64691579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100860315-C-A

64691579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100860315-C-G

64691579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100860315-C-T

64691689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100860410-A-G

64691704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100860425-G-A

64691761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100860445-G-A

64691761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100860445-G-T

64691819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100860493-T-C

64691881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100860549-A-G

http://identifiers.org/hco/1/GRCh38#64691950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100860608-C-A

64691970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100860628-A-G

64692025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100860680-G-A

64692025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100860680-G-T

64692036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100860691-T-C

http://identifiers.org/hco/1/GRCh38#64692260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100860900-C-A

64692380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100861088-G-A

64692493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100861199-G-A

64692493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100861199-G-T

64692518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100861224-G-T

64692565-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100861271-T-A

64692565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100861271-T-C

64692613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100861322-G-A

64692833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100861521-A-G

64692844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100861533-A-G

64692873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100861551-G-A

64692873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29314
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100861551-G-C