82358594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 105677141-C-T

82358683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105677052-G-C

82358768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105676973-A-G

82358768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105676973-A-T

82358776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105676965-G-A

82358792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105676958-C-G

82358792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105676958-C-T

82358813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105676946-A-G

82358813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105676946-A-T

http://identifiers.org/hco/12/GRCh38#82358904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#105676872-C-A

82358904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 105676872-C-T

http://identifiers.org/hco/12/GRCh38#82358966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105676813-C-A

82358966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676813-C-G

82358966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676813-C-T

82358971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676808-T-G

82358983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676794-G-A

82358983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676794-G-C

82358983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676794-G-T

82359140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676664-A-G

82359423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676472-T-G

82359545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676433-G-A

82359546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676432-G-C

82359554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676424-C-T

82359773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676286-A-G

82360007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105676024-A-G

82360060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105675977-A-G

82360254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105675789-A-T

82381151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105673282-T-A

82381381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105673046-T-C

82381627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105672789-A-G

82381955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105672495-G-A

82382325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105672213-C-G

82382373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105672163-A-G

82382470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105672035-C-T

82382611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105671878-A-G

82383382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105671574-G-A

82383391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105671566-A-G

82383891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105671105-C-T

82384116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105670691-A-T

http://identifiers.org/hco/12/GRCh38#82384129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105670678-A-C

82384129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105670678-A-G

http://identifiers.org/hco/12/GRCh38#82384416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105670456-C-A

82384416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105670456-C-T

82384469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105670419-G-T

82384499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105670385-C-T

82384978-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105669919-T-G

82385080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105669837-A-G

82385142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105669770-G-T

82385146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105669766-A-G

82385401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105669532-T-C

82385454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105669483-G-A

82386746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105668918-T-G

82386870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105668807-T-C

82386942-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105668735-T-C

82386994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105668684-G-A

http://identifiers.org/hco/12/GRCh38#82387045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105668632-C-A

82387135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105668546-A-G

82387435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105668260-A-G

82387692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105667952-A-G

82387784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105667879-C-T

82387856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105667809-T-G

82387931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105667551-A-T

82388240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105667210-G-A

http://identifiers.org/hco/12/GRCh38#82388450-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105666995-A-C

82388812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105666696-G-A

82388812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105666696-G-T

82388813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105666695-C-T

http://identifiers.org/hco/12/GRCh38#82388983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105666611-C-A

82389036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105666559-T-C

http://identifiers.org/hco/12/GRCh38#82389076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105666509-C-A

http://identifiers.org/hco/12/GRCh38#82389342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105666270-C-A

82389614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105665992-T-C

82389621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105665985-C-T

82389778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105665857-G-T

82389785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105665850-T-C

82389954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105665690-A-G

82397901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105663569-G-A

82398046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105663439-G-A

82398107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105663364-T-C

82398270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105663165-G-T

82398326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105663099-C-T

82398457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105662754-C-T

82398507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105662708-G-C

82398649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105662571-T-G

82398670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105662550-G-T

82398693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105662525-A-G

82398729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105662484-A-G

http://identifiers.org/hco/12/GRCh38#82398736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105662477-A-C

82398736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105662477-A-G

82398801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105662444-G-T

82398846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105662399-A-G

82398846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 105662399-A-T

82398858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 105662387-A-T

82398894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105662351-C-G

82398894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105662351-C-T

82398946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105662299-A-G

82398980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105662265-A-G

82399028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105662217-A-G

82399036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105662209-C-G

82399082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 105662166-T-G

82399110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105662138-G-A

82399128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105662120-A-G

82399146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105662102-A-T

82399176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105662072-A-T

82399300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105661951-T-C

82399315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105661936-G-C

82399375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105661876-A-G

82399408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105661843-T-A

82399408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105661843-T-C

82399469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105661775-A-G

http://identifiers.org/hco/12/GRCh38#82399500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105661748-C-A

82399500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105661748-C-T

82399927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105661219-G-A

http://identifiers.org/hco/12/GRCh38#82399938-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105661208-C-A

82400420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105661071-G-A

82402064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105659812-G-T

82402072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105659804-A-G

http://identifiers.org/hco/12/GRCh38#82402263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105659613-A-C

82402338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105659556-A-T

82402542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105659349-A-G

http://identifiers.org/hco/12/GRCh38#82402598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105659294-A-C

82402598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105659294-A-G

http://identifiers.org/hco/12/GRCh38#82402747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105659223-A-C

82402747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105659223-A-G

82402747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105659223-A-T

82402972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105659179-G-A

82402991-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105659161-G-C

82403164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105658987-A-G

http://identifiers.org/hco/12/GRCh38#82403282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105658500-C-A

82403282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105658500-C-T

http://identifiers.org/hco/12/GRCh38#82403310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105658472-A-C

82403310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105658472-A-G

82403378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105658403-A-G

http://identifiers.org/hco/12/GRCh38#82408051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105657264-C-A

http://identifiers.org/hco/12/GRCh38#82408052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105657263-C-A

82408077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105657240-T-G

82408308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105657007-C-T

82408489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105656848-C-G

82408776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655801-T-C

82408851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655732-T-C

82408918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655670-T-C

82408920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655668-T-C

82409022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655580-A-G

82409068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655534-T-C

82409165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655436-G-T

82409368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105655242-T-C

82410117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 105653875-A-G

82411980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105652653-A-G

82411983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105652650-G-A

82411983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105652650-G-C

82412050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105652593-T-G

http://identifiers.org/hco/12/GRCh38#82412098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105652548-A-C

82412099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105652547-G-T

82412217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105652360-T-C

82412259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105652321-T-C

82413546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105643429-G-A

82413763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105643212-A-G

82413927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105643077-C-T

82414251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105642764-A-G

82414362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105642659-A-G

82414746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641993-T-G

82414976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641785-G-A

82414984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641779-T-G

82415009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641751-A-G

82415085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641673-T-A

82415278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641505-A-G

82415294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641489-T-C

82415355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641428-A-G

82415355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641428-A-T

82415456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641210-C-T

82415583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641092-A-G

82415663-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105641012-T-G

82415748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640930-C-G

82415748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640930-C-T

82415853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640827-C-T

82415874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640806-A-G

82415950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640736-T-A

82415950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640736-T-C

82416200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640548-C-T

http://identifiers.org/hco/12/GRCh38#82416234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105640516-A-C

82416322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640450-T-G

82416440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640334-A-T

82416465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105640312-A-T

82425380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105640166-G-A

82425417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 105640131-G-T

82425518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105639951-G-A

82425518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105639951-G-T

82425812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105639574-A-G

82426115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105639258-G-A

82426346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105639068-A-G

82426382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105639032-G-A

82426489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105638955-C-T

82428527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105634547-C-T

82428631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105634443-A-G

82428692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105634383-A-G

82428698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105634377-C-T

82428819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105634285-C-T

82429956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105634074-T-A

82430163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105633878-T-G

82430401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105633667-G-A

82430401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105633667-G-T

82430404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105633664-C-T

82430513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105633562-A-G

82430762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105633311-A-G

http://identifiers.org/hco/12/GRCh38#82430766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105633302-C-A

82430812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105633257-T-C

82430845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105633224-A-G

82430888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105633183-T-C

http://identifiers.org/hco/12/GRCh38#82430901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105633170-C-A

82430901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 105633170-C-T

82430907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105633164-A-G

82430967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105633104-G-A

82431087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105632989-A-G

82431111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105632901-T-G

82431148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105632822-C-G

82431153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105632817-T-C

http://identifiers.org/hco/12/GRCh38#82431220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105632728-A-C

82431240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105632703-A-G

82431339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105632626-T-C

82431431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105632529-A-G

82431562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105632399-T-C

82431663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105632317-A-G

82432106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105632229-T-C

82432169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105632166-G-T

82432347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631974-G-A

82432363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631958-T-C

82432385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631937-T-A

82432385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631937-T-C

82433661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631685-T-C

82433806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631541-T-C

82433899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631452-T-A

82433949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631392-T-C

82433949-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105631392-T-G

http://identifiers.org/hco/12/GRCh38#82434555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105630391-C-A

82434566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630381-G-A

82434566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630381-G-T

http://identifiers.org/hco/12/GRCh38#82434577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105630370-C-A

82434577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630370-C-T

82434583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630364-A-G

http://identifiers.org/hco/12/GRCh38#82434586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105630361-A-C

82434586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630361-A-G

82434641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630307-A-G

http://identifiers.org/hco/12/GRCh38#82434656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105630292-C-A

82434658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630290-A-G

82434892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105630046-C-T

82436341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105629940-C-T

82436440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105629835-T-A

82436440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105629835-T-G

82436499-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105629774-T-A

82436726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105629546-A-G

http://identifiers.org/hco/12/GRCh38#82438780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105629210-C-A

82438780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 105629210-C-T

82448632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105625523-T-G

82448705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105625444-A-G

82448717-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105625432-A-T

82449059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105625136-G-A

82449438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105624776-A-G

82449492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105624724-C-G

82449561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105624665-C-T

82449662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105624574-C-T

82450754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623944-A-G

82450809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623898-G-T

82450856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623871-G-T

82450858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623869-T-A

82450902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623821-A-G

82450944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623782-T-A

82450951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623775-G-T

82451083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623652-T-C

82451203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623545-G-T

http://identifiers.org/hco/12/GRCh38#82451223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105623525-C-A

82451224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623524-T-C

82451228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623520-T-C

82451229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623519-G-A

82451233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623515-T-C

82451235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623513-T-A

82451235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623513-T-C

82451244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623504-T-C

82451264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623487-T-C

http://identifiers.org/hco/12/GRCh38#82451299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105623455-C-A

82451299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623455-C-T

82451397-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623281-A-T

82451454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623224-A-G

82451514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623179-A-G

82451650-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623078-C-G

82451650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105623078-C-T

82451916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105622836-A-G

82452271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105621167-T-C

82452304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105621125-T-C

82452311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105621118-T-A

82453535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105620698-G-T

82453651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105620641-C-T

http://identifiers.org/hco/12/GRCh38#82453767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105620538-C-A

82453767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105620538-C-T

82453852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105620462-G-A

82453852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105620462-G-C

82453973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105620287-C-T

82454325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105619946-G-A

82454378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105619890-G-A

82454461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105619705-T-G

82455021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105618501-G-A

82455033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105618489-G-T

82455186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105618354-C-G

http://identifiers.org/hco/12/GRCh38#82455214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105618327-A-C

82455356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105618211-G-T

http://identifiers.org/hco/12/GRCh38#82455458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105618109-C-A

82455474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105618092-T-C

82455494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105618074-C-T

82455607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105617978-G-A

82455650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105617937-G-A

82455693-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105617897-T-G

82456111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105616136-G-A

82456111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105616136-G-T

82456164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105616072-A-G

82456644-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615623-T-G

82456706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615561-T-G

82456853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615414-A-G

http://identifiers.org/hco/12/GRCh38#82456893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105615375-C-A

82456893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615375-C-G

82456916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615352-T-A

82456916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615352-T-G

82457070-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615203-T-A

82457171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105615111-A-G

http://identifiers.org/hco/12/GRCh38#82457663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105614860-C-A

82457663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105614860-C-T

82457688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105614838-T-C

82458190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105614492-C-T

82458550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105614251-G-C

http://identifiers.org/hco/12/GRCh38#82458574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105614226-C-A

82458574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105614226-C-T

http://identifiers.org/hco/12/GRCh38#82458593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105614207-C-A

82458593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105614207-C-T

82458909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105613964-C-T

82459178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105613737-T-A

82459213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105613709-G-A

http://identifiers.org/hco/12/GRCh38#82459302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105613619-A-C

82459318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105613601-G-A

82459850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105609573-A-G

82459869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 105609555-A-G

http://identifiers.org/hco/12/GRCh38#82460101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105605294-C-A

http://identifiers.org/hco/12/GRCh38#82476528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105602019-C-A

http://identifiers.org/hco/12/GRCh38#82476578-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105601971-A-C

82476578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105601971-A-G

82476607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 105601936-A-G

82476665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105601876-A-G

82476707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105601834-G-A

82476707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105601834-G-T

82476792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601711-T-C

http://identifiers.org/hco/12/GRCh38#82476824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105601594-C-A

82476837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601581-G-T

82476915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601501-A-T

http://identifiers.org/hco/12/GRCh38#82477051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105601364-C-A

82477162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601252-G-T

82477175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601239-A-G

82477175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601239-A-T

http://identifiers.org/hco/12/GRCh38#82477224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105601189-A-C

82477244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601179-G-A

82477244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105601179-G-T

http://identifiers.org/hco/12/GRCh38#82477332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105601099-C-A

82477332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105601099-C-T

82478045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105600409-T-C

82478076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105600381-T-C

82478176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105600286-A-G

82478305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105600160-T-C

82478428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105600040-T-A

82478568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105599918-A-G

82478819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105599673-G-T

82478882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105599369-T-C

82478882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105599369-T-G

82478898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105599354-T-A

http://identifiers.org/hco/12/GRCh38#82478915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#105599337-C-A

82478936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105599316-A-G

82478950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105599302-G-A

82479192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105599089-G-A

82479192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26228
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105599089-G-T