http://identifiers.org/hco/15/GRCh38#79431695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89505436-C-A

79432156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89504982-C-T

79432491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89504718-G-A

79432491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89504718-G-T

79432497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89504712-G-A

79432560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89504648-G-A

79432623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89504581-G-A

79432623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89504581-G-T

79432662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89504545-T-C

79432682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89504525-T-C

79432717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89504493-T-A

79432743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89504467-G-A

79432839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89504275-G-A

79432912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89504201-A-T

79432976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron_variant, undefined
orthologous variants: 89504137-G-A

79432989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89504124-T-C

79433392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89503753-G-A

http://identifiers.org/hco/15/GRCh38#79433801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89503399-C-A

79433944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89503259-T-A

79433958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89503245-A-G

http://identifiers.org/hco/15/GRCh38#79434359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89502816-C-A

79434359-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89502816-C-G

79435355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89502117-C-G

79436944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 112804604-A-G

79437303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 146343941-G-A

79437362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 146343875-A-G

79437413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 146343817-A-G

79437493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 146343721-G-A

79437538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 146343675-G-C

79437581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 146343632-G-C

79437581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 146343632-G-T

79437658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 146343554-T-A

79437658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 146343554-T-G

http://identifiers.org/hco/15/GRCh38#79437726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89500630-A-C

79437726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500630-A-G

79437726-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500630-A-T

79437731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500625-G-T

79437740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500619-G-T

79437742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500617-G-A

79437742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500617-G-T

79437744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500615-G-C

79437744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500615-G-T

79437748-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500611-G-C

79437748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500611-G-T

79437848-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500535-G-C

79437853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500530-T-A

79437853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500530-T-C

79437853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500530-T-G

79437911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500475-G-T

79437926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500458-G-A

79437928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500456-G-T

79437931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500453-T-C

79437931-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500453-T-G

79437950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500433-T-C

79437950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500433-T-G

79437956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500427-G-A

79437979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500396-G-T

79438038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500330-G-T

79438126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500238-G-A

79438318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: -A-G

79438400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500027-A-G

79438422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500003-G-C

79438422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89500003-G-T

79438445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89499985-G-T

79438446-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89499984-T-G

79438469-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89499956-T-G

79438533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89499891-G-A

79438560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89499864-T-G

79438736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89499700-G-A

79438781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89499661-T-G

79438793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89499649-C-G

79438847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89499603-G-C

79442111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89498547-C-G

http://identifiers.org/hco/15/GRCh38#79442167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89498488-C-A

79442167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89498488-C-G

79442167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89498488-C-T

79442254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89498404-G-A

79442513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89498178-A-G

http://identifiers.org/hco/15/GRCh38#79442581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89497897-C-A

79442581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89497897-C-T

79442896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89497558-T-C

http://identifiers.org/hco/15/GRCh38#79443163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89497344-C-A

79443228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89497309-G-A

79443228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89497309-G-C

79443488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89497052-T-C

79443564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89496981-T-G

79443722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89496870-T-C

79443733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89496856-A-G

http://identifiers.org/hco/15/GRCh38#79447686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89494077-C-A

79448167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89493706-T-A

79448484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89493390-C-T

79448619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89493269-T-C

79448675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89493240-G-T

79448745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89493184-A-G

79448922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89492995-A-G

79449076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89492725-G-T

79449236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89491822-G-T

79449271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89491788-C-T

http://identifiers.org/hco/15/GRCh38#79449277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89491782-C-A

79449384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89491688-C-T

79449459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89491613-G-A

79449459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89491613-G-C

79449875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89491300-C-G

79449960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89491221-A-G

79450151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89491031-A-G

79450433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89490715-T-C

79453911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89488896-A-G

79453912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89488895-T-A

79454177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89488470-T-C

79454246-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89488401-C-G

79454742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89486009-A-G

79454820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89486304-C-T

79454827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89486311-G-C

79454902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89486384-A-G

79455270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89486748-A-T

79455511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 89486972-A-T

79455701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: 89485842-G-A

79455711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89485832-T-G

79455807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89485733-T-C

79456019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89485519-T-C

http://identifiers.org/hco/15/GRCh38#79456028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89485510-C-A

79456028-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89485510-C-G

79456028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: intron variant
orthologous variants: 89485510-C-T

79456406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89485135-A-T

79456465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 89485076-C-T

79456466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89485075-A-T

79456496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89485045-G-A

79456512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89485029-G-A

79456512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89485029-G-T

79456697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 89484844-G-T

http://identifiers.org/hco/15/GRCh38#79456705-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89484836-A-C

79456958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89484583-T-A

79456958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89484583-T-C

http://identifiers.org/hco/15/GRCh38#79456981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89484560-C-A

79456981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89484560-C-G

79456996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 89484545-T-C

79457006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, stop_gained
orthologous variants: 89484535-G-T

79457118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89484423-G-A

79457118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89484423-G-C

79457122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 89484419-A-G

79457327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89484214-C-T

79457435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89484106-G-A

79457439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89484102-A-G

79457474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89484067-C-T

79457483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 89484058-C-T

79457888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89483650-C-T

79458056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89483482-C-T

http://identifiers.org/hco/15/GRCh38#79458260-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89483278-A-C

79458515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89483053-G-A

79458515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89483053-G-T

79458521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89483047-G-A

79458551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89483011-G-A

79458551-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89483011-G-C

79458551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89483011-G-T

http://identifiers.org/hco/15/GRCh38#79458853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89482712-C-A

79459275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89482535-A-G

79459280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89482530-G-A

79459310-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89482508-T-G

http://identifiers.org/hco/15/GRCh38#79459451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89482378-C-A

http://identifiers.org/hco/15/GRCh38#79459485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89482345-C-A

79459487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89482343-A-G

79459660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89482166-G-A

79459718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89482111-A-T

http://identifiers.org/hco/15/GRCh38#79459981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89481951-A-C

79460077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89481908-G-C

79460077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89481908-G-T

79460160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89481829-T-A

79460163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89481826-G-A

79460411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89481591-G-A

79460411-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89481591-G-C

http://identifiers.org/hco/15/GRCh38#79460435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89481570-C-A

79460522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89481484-C-T

79460643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89481342-G-T

79460702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89481284-C-G

79460793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89481006-G-A

79460793-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89481006-G-T

79461137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89480476-T-C

79461138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89480475-A-G

79461151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89480460-G-T

79461527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89480084-G-A

79461551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89480052-A-G

79461781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89479862-C-T

http://identifiers.org/hco/15/GRCh38#79461888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#89479839-A-C

79462281-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89479605-G-C

79462477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89479338-C-T

79462542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89479270-C-G

79462635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89479184-C-T

79462849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89478964-G-A

79462923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89478901-A-G

79462923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89478901-A-T

79463019-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89478789-C-G

79463019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89478789-C-T

79463223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89478585-G-A

79463223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 89478585-G-C

79463326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89478482-G-A

79463573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89478241-C-T

79463597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89478220-T-A

79463597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 89478220-T-G

79463895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89477926-G-T

79463992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89477845-A-G

79464130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89477712-G-A

79464222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89477633-G-A

http://identifiers.org/hco/15/GRCh38#79464362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#89477486-A-C

79464563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89477286-G-A

79464814-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89476976-G-C

79464943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant, undefined
orthologous variants: 89476756-A-G

79464964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89476735-G-A

79464972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89476727-G-A

79465101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89476612-T-C

79465340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89476387-C-T

79465500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89476234-G-A

79465500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89476234-G-C

79465500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89476234-G-T

79465824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89475908-G-A

79466116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89475335-G-A

79466116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89475335-G-T

79466273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89475217-T-C

79466417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89475156-T-C

79466709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89474883-G-A

79466777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89474780-G-C

79466908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89474643-G-C

79467096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89474504-T-A

79467777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89473910-T-A

79467809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89473878-G-T

79468135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89473403-G-T

79468307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, undefined
orthologous variants: 89473231-A-T

79468487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89473049-A-G

79468497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89473039-G-T

79468521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89473020-G-A

79468810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472739-G-A

79468810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472739-G-T

79468833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472717-T-C

79468846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472704-G-T

79468847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472703-G-T

79468877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472674-G-T

79468909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472642-T-C

79468953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472602-T-A

79468953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472602-T-G

79469016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472545-G-T

79469035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472526-G-T

79469068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472494-T-G

79469091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472471-A-G

79469128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472424-G-A

79469128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472424-G-T

79469133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472419-C-T

79469140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472415-T-C

79469140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472415-T-G

79469207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472348-T-C

79469233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472322-G-A

79469347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472221-T-G

79469501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89472092-G-A

79469671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89471945-G-C

http://identifiers.org/hco/15/GRCh38#79469731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#89471886-A-C

79469731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89471886-A-G

http://identifiers.org/hco/15/GRCh38#79469757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#89471860-A-C

79469792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89471825-C-T

79469965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89471650-G-A

79469993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89471623-G-A

79470176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89471450-G-A

79470178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89471411-A-G

79470296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89471285-G-T

79470312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89471269-T-C

http://identifiers.org/hco/15/GRCh38#79470414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#89471166-C-A

79470414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89471166-C-T

http://identifiers.org/hco/15/GRCh38#79470543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#89471009-C-A

79470656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89470916-A-G

79470754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89470834-T-A

79470754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89470834-T-C

http://identifiers.org/hco/15/GRCh38#79470998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#89470616-C-A

79471085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89470540-T-C

79471090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89470535-A-G

79471093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 89470532-T-G

http://identifiers.org/hco/15/GRCh38#79471270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#89470379-C-A

http://identifiers.org/hco/15/GRCh38#79471400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#89470133-A-C

79471400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89470133-A-G

79471413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89470120-A-G

http://identifiers.org/hco/15/GRCh38#79471437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#89470086-C-A

79471437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89470086-C-T

79471777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89469777-G-A

79471892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89469655-T-C

79472013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89469539-T-C

79472048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 89469504-A-T

http://identifiers.org/hco/15/GRCh38#79472128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29172
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#89469426-C-A