112597505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: 44949777-G-T

112597543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: 44949730-G-T

http://identifiers.org/hco/3/GRCh38#112597571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44949702-C-A

112597587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: 44949686-C-T

112597774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: 44949487-A-T

http://identifiers.org/hco/3/GRCh38#112597809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44949439-C-A

112597882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: 44949394-T-C

112597984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: 44949295-T-C

http://identifiers.org/hco/3/GRCh38#112598097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44949186-C-A

112598129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: 44949151-C-T

112604989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: 44948297-G-A

112604989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: 44948297-G-T

112605025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: 44948261-T-C

http://identifiers.org/hco/3/GRCh38#112605186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44948090-A-C

112605186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: 44948090-A-G

112605186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3 prime UTR variant
orthologous variants: 44948090-A-T

112605274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 44948017-G-A

112605355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 44947933-G-A

112605355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 44947933-G-T

112605360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 44947928-A-G

http://identifiers.org/hco/3/GRCh38#112605843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44947448-C-A

112605843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44947448-C-T

112605969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44947334-C-G

112606178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44947131-T-C

112606789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44946871-T-C

112607029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44946661-G-A

112607029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44946661-G-T

http://identifiers.org/hco/3/GRCh38#112607084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44946627-C-A

112607086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44946625-T-A

112607086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44946625-T-G

112607096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44946615-C-T

http://identifiers.org/hco/3/GRCh38#112607108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44946603-A-C

112607108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44946603-A-G

112607329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44946404-T-C

112607329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44946404-T-G

http://identifiers.org/hco/3/GRCh38#112607342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44946390-A-C

112607395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44946337-C-G

http://identifiers.org/hco/3/GRCh38#112608348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44945139-A-C

112608355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44945132-T-A

112608362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44945119-T-C

112608396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44945086-T-C

112608500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44944990-T-C

112608523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44944968-C-T

112608535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44944956-G-A

112608571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44944920-C-T

112608642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44944715-G-T

112608924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44944438-G-C

112608970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44944189-C-T

112609077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44944075-A-G

112609139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44944017-G-T

112609310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44943856-G-A

112609615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44943609-A-G

112609616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44943608-T-C

112609865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44943404-A-G

112609945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44943343-G-A

112609945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44943343-G-T

112610098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 44943193-G-A

112610102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 44943189-A-G

http://identifiers.org/hco/3/GRCh38#112610138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44943157-A-C

112610138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 44943157-A-G

http://identifiers.org/hco/3/GRCh38#112610252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44943046-C-A

112610338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44942981-T-C

112610535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44942793-A-G

http://identifiers.org/hco/3/GRCh38#112611462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44942225-A-C

112611696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44942040-A-T

112611943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44941814-A-T

112612157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44941611-G-T

112612446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44941352-T-C

112612783-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44941016-C-G

112612844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44940956-T-G

112612974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44940829-C-G

112615166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44939695-G-A

112615190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44939674-A-G

112615190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44939674-A-T

http://identifiers.org/hco/3/GRCh38#112615208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44939656-C-A

112615401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44939473-G-A

112616206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44939242-A-G

112616249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44939199-T-C

112616407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44939060-G-A

112616409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44939058-T-G

112616477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44939018-A-G

http://identifiers.org/hco/3/GRCh38#112616572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44938936-C-A

112616572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44938936-C-T

http://identifiers.org/hco/3/GRCh38#112616574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44938934-A-C

http://identifiers.org/hco/3/GRCh38#112616576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44938932-A-C

http://identifiers.org/hco/3/GRCh38#112616595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44938925-C-A

112616595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44938925-C-T

112616691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44938629-G-A

112616691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44938629-G-T

112616954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44938409-G-C

112616954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44938409-G-T

112617232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44938127-G-A

112617371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44938027-A-T

112617398-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44938000-A-T

112617584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44937852-C-G

112617613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44937819-C-T

112618034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44937565-T-C

http://identifiers.org/hco/3/GRCh38#112618642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44937045-C-A

112618668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44937019-C-T

112618743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44936948-C-T

http://identifiers.org/hco/3/GRCh38#112618853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44936838-C-A

112618926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44936784-T-G

112618936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44936774-A-G

112618984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44936727-A-G

112619010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: synonymous variant
orthologous variants: 44936701-A-G

112619041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44936670-T-G

112619056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44936655-T-C

112619084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44936627-C-G

112619084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44936627-C-T

http://identifiers.org/hco/3/GRCh38#112619105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: splice acceptor variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44936606-C-A

112619105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: splice acceptor variant
orthologous variants: 44936606-C-T

112619130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44936581-A-G

http://identifiers.org/hco/3/GRCh38#112619152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44936559-A-C

http://identifiers.org/hco/3/GRCh38#112619154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44936557-C-A

112619229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44936471-T-C

http://identifiers.org/hco/3/GRCh38#112619377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44936304-A-C

112619676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44936024-G-C

112619780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44935932-G-T

112620330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44934253-T-C

http://identifiers.org/hco/3/GRCh38#112620622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44933903-C-A

http://identifiers.org/hco/3/GRCh38#112621933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44932479-A-C

112621933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44932479-A-G

112621938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44932463-T-C

112621979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44932422-C-T

112622032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44932362-G-A

112622032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44932362-G-C

112622549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44931843-A-G

112625731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44929421-T-A

112625930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44929267-A-G

112625930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44929267-A-T

112626131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44928883-T-C

http://identifiers.org/hco/3/GRCh38#112626213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44928817-A-C

112626233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44928797-T-C

112626328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44928708-C-T

112626517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44928519-C-T

112626931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44928427-C-T

112626971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44928382-A-G

http://identifiers.org/hco/3/GRCh38#112627208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44928110-C-A

112627863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44927468-G-A

112627863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44927468-G-C

112627863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44927468-G-T

112627891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44927441-G-A

112627891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44927441-G-C

http://identifiers.org/hco/3/GRCh38#112628193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44927142-C-A

112628193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44927142-C-T

112628517-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44926815-T-G

http://identifiers.org/hco/3/GRCh38#112628564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44926758-A-C

112629024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44926146-G-T

http://identifiers.org/hco/3/GRCh38#112629125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44926061-A-C

112629125-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44926061-A-T

112629126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44926060-T-A

112629329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44925830-G-A

112629329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44925830-G-C

112629440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44925649-C-T

112629457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44925634-C-T

http://identifiers.org/hco/3/GRCh38#112629940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44925193-C-A

112630016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44925053-T-C

112630016-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44925053-T-G

112630345-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44924668-T-A

http://identifiers.org/hco/3/GRCh38#112630421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44924605-A-C

112630593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44924433-G-A

112631153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44923818-G-A

112631319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44923668-C-T

112631323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44923664-G-A

112631389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44923599-A-G

112631630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, undefined
orthologous variants: 44923426-G-A

112631802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44923257-T-C

112632117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44922951-A-G

http://identifiers.org/hco/3/GRCh38#112632332-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44922764-A-C

112632390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44922723-A-G

112632424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44922691-T-G

112633142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44922108-A-G

112633142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44922108-A-T

112633257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44922042-C-T

112633280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44922018-G-A

112633690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44921620-A-G

112633690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44921620-A-T

112633786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44921527-A-G

112633842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44921471-A-G

112633842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44921471-A-T

112633846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44921467-C-T

112633848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44921465-C-G

112633918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44921399-T-G

112634081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44921234-G-A

112634427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44920575-A-G

112634460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44920540-C-T

112634641-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44920361-C-G

112634642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44920360-A-T

112634698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44920274-T-C

112634704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44920239-A-G

112634818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44920026-C-T

112634829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44920015-G-A

112635372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44919472-T-G

112635440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44919403-G-A

112635488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44919356-A-T

112635753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44919129-T-A

112635759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44919123-G-A

112635896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44918985-C-G

112636117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44918757-T-G

112636514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44918256-T-C

112636863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44917930-C-T

112636883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44917910-T-C

http://identifiers.org/hco/3/GRCh38#112636961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44917823-C-A

112636961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44917823-C-T

112637201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44917561-C-G

112637327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44917442-T-C

112637951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron variant
orthologous variants: 44917189-T-G

112638065-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44917081-T-A

http://identifiers.org/hco/3/GRCh38#112638140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44917006-C-A

112638177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44916969-T-C

112638288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44916858-G-A

112638363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44916783-G-A

112638363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44916783-G-T

112638465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44916687-C-G

112638465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44916687-C-T

112638483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44916669-G-A

112638638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44916514-T-G

112638738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44916414-G-A

112638739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: synonymous variant
orthologous variants: 44916413-G-C

112638739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: synonymous variant
orthologous variants: 44916413-G-T

112639016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44916133-C-T

http://identifiers.org/hco/3/GRCh38#112639043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44916106-C-A

112639043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44916106-C-T

http://identifiers.org/hco/3/GRCh38#112639382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44915767-A-C

112639382-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44915767-A-G

112639382-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense variant
orthologous variants: 44915767-A-T

112639478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44915671-G-A

112639565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44915584-G-A

112639568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44915581-G-A

112639604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44915545-G-A

112639736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44915413-C-T

112639797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 44915352-T-C

112639804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 44915345-T-C

112639933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 44915216-G-C

http://identifiers.org/hco/3/GRCh38#112640052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44915070-A-C

112640288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44914817-A-G

112640304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44914809-G-A

112640353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44914761-G-C

112640353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44914761-G-T

http://identifiers.org/hco/3/GRCh38#112640368-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44914746-A-C

112640368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44914746-A-G

112640368-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44914746-A-T

112640410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44914705-C-T

112640492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44914660-G-A

112640492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44914660-G-T

112640663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44914520-C-T

http://identifiers.org/hco/3/GRCh38#112640805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44914376-C-A

112640805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44914376-C-T

112640806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 44914375-G-A

112641125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44914027-A-G

112641126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44914026-G-C

112641126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 44914026-G-T

112641158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44913996-G-A

112641158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44913996-G-T

112641296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 44913854-T-A

http://identifiers.org/hco/3/GRCh38#112641345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44913809-C-A

112641345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44913809-C-T

112641375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44913779-C-T

112641688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44913476-C-G

112641697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44913472-C-T

112641792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44913339-A-G

112641833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44912676-G-A

112642083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44912437-T-A

112642083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44912437-T-C

http://identifiers.org/hco/3/GRCh38#112642122-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44912391-A-C

http://identifiers.org/hco/3/GRCh38#112642184-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44912328-A-C

112642668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44911005-G-C

112643129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44910512-C-T

112643348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 44910342-G-T

112643527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44910178-G-T

112643618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44909941-A-G

112643698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44909866-T-C

112643879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44909411-T-G

112643937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44909344-A-G

112645967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44907422-G-C

112645967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44907422-G-T

112645974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44907415-A-G

http://identifiers.org/hco/3/GRCh38#112646075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44906021-C-A

112646075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44906021-C-G

112646136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44905967-A-G

http://identifiers.org/hco/3/GRCh38#112646307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44905796-A-C

112646307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44905796-A-G

112646344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44905759-A-T

112646666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44905434-C-G

112646666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44905434-C-T

112646781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44905300-T-G

112647197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44902670-A-G

112647448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44902446-G-A

112647475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44902419-G-C

112647514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 44902380-G-A

112648206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44901669-T-C

112648213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44901662-G-A

112648500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44901400-C-T

112648713-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44901249-A-T

112648778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44901158-G-A

112648778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44901158-G-T

112648879-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44898682-T-G

112648957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44898603-T-C

112649267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44898427-T-C

http://identifiers.org/hco/3/GRCh38#112649281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#44898413-C-A

112649281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44898413-C-T

112649305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 44898389-A-G

112649369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: non coding transcript exon variant
orthologous variants: 44898332-G-A

112649369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: non coding transcript exon variant
orthologous variants: 44898332-G-T

112649406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30649
most severe consequence: non coding transcript exon variant
orthologous variants: 44898253-A-T