48716843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125397416-C-G

48716909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125397475-T-C

48716967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125397532-T-C

48717632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125397912-G-A

48717795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125398068-G-A

48718016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125398213-G-A

48718156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125398310-G-C

48718324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125398469-C-T

48718386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125398552-G-A

48719607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125399406-A-T

48720107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125399811-G-C

http://identifiers.org/hco/15/GRCh38#48720122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125399826-C-A

48720122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125399826-C-T

48720653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125400338-A-G

48720740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125400449-T-C

48720762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125400476-G-T

48720852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125400560-T-G

48720914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125400625-G-T

http://identifiers.org/hco/15/GRCh38#48720915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125400626-A-C

48720943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125400654-A-G

48720958-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125400669-T-A

48721245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125400900-G-C

48721295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125400951-G-A

48721592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125401229-G-T

48721734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125401347-A-G

48721741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125401354-A-G

48721942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125401568-A-T

48722121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125401728-A-G

48722174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125401779-C-G

48722447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125402030-A-G

http://identifiers.org/hco/15/GRCh38#48722459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125402042-A-C

48724809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 125402741-T-C

48737941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125405011-A-T

http://identifiers.org/hco/15/GRCh38#48737988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125405057-C-A

48738060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125405129-A-T

http://identifiers.org/hco/15/GRCh38#48738065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125405135-C-A

48738065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125405135-C-G

http://identifiers.org/hco/15/GRCh38#48738090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125405158-A-C

48738090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125405158-A-T

http://identifiers.org/hco/15/GRCh38#48738149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125405210-C-A

48738149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125405210-C-G

48738149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125405210-C-T

48738267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 125405329-T-C

48738267-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 125405329-T-G

48738407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125405469-G-C

http://identifiers.org/hco/15/GRCh38#48738427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125405489-A-C

48738430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125405492-T-C

48738532-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125405579-A-T

http://identifiers.org/hco/15/GRCh38#48738702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125405746-A-C

http://identifiers.org/hco/15/GRCh38#48738806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125405850-C-A

48738806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125405850-C-T

48738898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125405927-G-A

http://identifiers.org/hco/15/GRCh38#48738909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125405938-C-A

48738909-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 125405938-C-G

48738909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 125405938-C-T

48739023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 125406049-T-A

48739024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125406050-A-G

48739085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125406111-G-T

http://identifiers.org/hco/15/GRCh38#48739132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125406158-C-A

48739132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125406158-C-T

48739162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125406188-C-T

48739318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125406344-G-A

48740320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407125-C-G

http://identifiers.org/hco/15/GRCh38#48740799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125407638-C-A

48740799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407638-C-T

48740845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407685-T-A

48740845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407685-T-C

48740868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407760-A-G

48740877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407769-G-A

48740877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407769-G-T

48740911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407817-G-A

48740911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407817-G-T

http://identifiers.org/hco/15/GRCh38#48740956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125407856-A-C

48740956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407856-A-G

48740956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407856-A-T

48741013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407911-G-A

48741013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407911-G-T

http://identifiers.org/hco/15/GRCh38#48741072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125407954-C-A

48741072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125407954-C-T

http://identifiers.org/hco/15/GRCh38#48741440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125408076-C-A

48741568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125408118-A-G

48741602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 125408153-T-C

48741752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125408293-G-T

http://identifiers.org/hco/15/GRCh38#48741919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125408425-C-A

48741919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125408425-C-T

48741921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125408427-G-A

http://identifiers.org/hco/15/GRCh38#48741927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125408433-A-C

48741927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125408433-A-T

48741928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125408434-T-C

48741928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125408434-T-G

48741931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125408437-T-C

48742012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125408521-G-A

48742012-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125408521-G-C

48742042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125408551-T-A

48742084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125408593-A-G

48742104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125408613-T-C

48742111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125408617-G-A

48742220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125408710-A-T

48742229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125408719-T-C

48743176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125409800-C-T

48743334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125409936-T-C

48744196-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125410697-A-T

48744208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125410709-G-A

http://identifiers.org/hco/15/GRCh38#48744297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125410801-C-A

48744297-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125410801-C-G

48744307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125410811-C-T

48744890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411469-G-A

48744890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411469-G-T

48744928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125411507-T-C

48744939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125411518-T-G

48744980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125411559-T-G

48745066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411620-A-G

48745084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411637-G-C

48745084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125411637-G-T

48745879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125412211-G-T

48745992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125412307-G-C

http://identifiers.org/hco/15/GRCh38#48746258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125412516-C-A

48746258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125412516-C-T

48747902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413369-C-T

48748393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413555-C-G

48748395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413557-A-G

48748461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125413607-C-T

48748494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125413640-G-T

http://identifiers.org/hco/15/GRCh38#48748682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125413832-A-C

48748682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413832-A-G

48748703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413853-G-A

48748703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413853-G-T

48748746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125413886-C-T

http://identifiers.org/hco/15/GRCh38#48748784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125413920-C-A

48749187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125414297-G-A

48749279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125414361-T-C

48749311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125414366-G-A

48749982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125415276-T-G

48750304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125415594-T-A

48750304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125415594-T-C

http://identifiers.org/hco/15/GRCh38#48750425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125415725-C-A

48752371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125418656-T-C

48752429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125418735-C-T

http://identifiers.org/hco/15/GRCh38#48752443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125418749-A-C

48752443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125418749-A-T

48752453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125418759-A-G

48752458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125418764-G-A

48752482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125418788-A-G

48752491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125418797-G-T

48752525-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125418843-T-A

48752578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125418910-T-C

http://identifiers.org/hco/15/GRCh38#48753728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125419370-A-C

48753728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125419370-A-G

48754033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125419637-T-C

48754434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125420014-T-C

48754566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125420176-G-A

48754782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125420364-C-T

48754955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125420532-A-G

48754995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125420572-T-C

48755059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125420625-G-T

48755104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125420668-C-T

48755171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125420708-T-C

48755171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125420708-T-G

48755191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125420728-A-G

48755637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125421045-G-C

48755770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125421175-T-A

http://identifiers.org/hco/15/GRCh38#48755806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125421210-C-A

48755806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125421210-C-T

48755807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125421211-T-C

48755865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125421266-T-C

48755925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125421316-T-C

http://identifiers.org/hco/15/GRCh38#48755974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125421365-C-A

48756078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125421469-G-T

48756079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125421470-T-C

48756084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125421475-C-G

48756093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125421484-A-G

48756129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125421520-T-C

48756236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125421627-T-C

http://identifiers.org/hco/15/GRCh38#48756452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125421843-A-C

http://identifiers.org/hco/15/GRCh38#48756455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125421846-A-C

48756455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125421846-A-T

48756467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125421858-C-T

48759102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125422411-A-G

48759336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125422603-C-T

48759351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125422618-G-A

48759821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125423061-G-A

48759891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125423123-G-T

48760117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125423598-T-C

48760270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125423751-T-C

48760321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125423782-T-C

48760365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125423825-A-G

48760419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125423863-A-G

48760455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125423897-G-C

48760455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125423897-G-T

48760639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125424079-C-T

48760907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125424513-T-C

48761829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125425197-T-C

48762304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125425636-T-C

48762349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125425677-A-G

48762436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125425757-G-A

48762436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125425757-G-T

48762465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125425786-T-C

48762518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125425827-A-G

48762560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125425872-A-T

48762599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125425911-T-C

48762805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125426245-G-A

48762805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125426245-G-T

48762824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125426264-T-C

http://identifiers.org/hco/15/GRCh38#48762944-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125426382-A-C

48763077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125426524-A-G

48763114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125426560-C-T

48763337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125426789-G-C

48763773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125426910-C-G

48763892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125427767-G-C

48763892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125427767-G-T

48764013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125427899-A-T

48764357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 125428356-T-G

http://identifiers.org/hco/15/GRCh38#48766213-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125428896-A-C

48766927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429411-T-A

48766927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429411-T-C

48766952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429438-T-G

48766987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429471-G-A

48766987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429471-G-T

48767029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429502-G-C

48767029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429502-G-T

http://identifiers.org/hco/15/GRCh38#48767212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125429667-C-A

48767222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429677-A-G

48767231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429699-C-T

48767251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429757-A-G

48767269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429773-C-T

http://identifiers.org/hco/15/GRCh38#48767448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/2/GRCm39#125429926-A-C

48767448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125429926-A-G

48767448-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 125429926-A-T

http://identifiers.org/hco/15/GRCh38#48767480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125429958-A-C

48767480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125429958-A-G

48767735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431055-T-C

48767781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431108-T-C

48767781-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431108-T-G

http://identifiers.org/hco/15/GRCh38#48767841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125431169-C-A

http://identifiers.org/hco/15/GRCh38#48768148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125431349-C-A

48768148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431349-C-T

48768151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431352-G-C

48768151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431352-G-T

48768161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431362-G-A

48768161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431362-G-T

48768239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125431396-G-A

48768239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125431396-G-T

48768242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125431399-A-G

48768336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125431493-C-G

48768495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431614-A-G

48768715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431822-T-C

48768766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431855-C-T

http://identifiers.org/hco/15/GRCh38#48768791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125431880-C-A

48768853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125431935-A-G

http://identifiers.org/hco/15/GRCh38#48768950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125432024-A-C

48768950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125432024-A-G

48768950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125432024-A-T

48768967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125432041-G-T

http://identifiers.org/hco/15/GRCh38#48768998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125432072-C-A

http://identifiers.org/hco/15/GRCh38#48769037-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125432108-A-C

48769037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125432108-A-G

48769135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125432205-C-G

48769308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125432373-C-T

http://identifiers.org/hco/15/GRCh38#48769408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125432459-A-C

48769596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125432664-G-A

48769600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125432668-G-A

48769748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125432795-A-G

48769986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125433031-G-T

48770889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125435875-C-T

48771011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125436000-A-G

48771013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125436002-G-A

48771022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125436011-G-A

48771339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125436312-T-C

48771642-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125436634-G-C

48772432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125436733-T-A

48772432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125436733-T-G

48772467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125436769-A-T

48772675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125436975-C-T

48772696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125436996-T-C

48772724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125437023-T-A

http://identifiers.org/hco/15/GRCh38#48772760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125437051-C-A

48772764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125437055-G-A

48772764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125437055-G-T

http://identifiers.org/hco/15/GRCh38#48772780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125437069-A-C

48772780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125437069-A-G

48772780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125437069-A-T

48772795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125437084-T-C

48777662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125440169-C-T

48777848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125440366-G-A

48777891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125440410-A-G

48778762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125441166-C-G

http://identifiers.org/hco/15/GRCh38#48778947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125441276-C-A

48778947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125441276-C-T

48778952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125441281-A-T

48779073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125441366-A-G

48779073-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125441366-A-T

48779345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125441596-C-T

48779941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125441928-C-T

48780078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125442046-C-T

48780175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125442138-T-A

48780193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125442151-A-G

48780287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125442242-T-C

48780336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125442290-T-C

http://identifiers.org/hco/15/GRCh38#48780752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125442630-C-A

48780752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125442630-C-T

48781029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125442907-T-G

http://identifiers.org/hco/15/GRCh38#48781224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125443097-C-A

48781224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125443097-C-G

48781224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125443097-C-T

48781266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125443139-T-C

48781433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125443301-T-A

48781495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125443364-T-C

48781807-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125444447-G-C

48782256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125444878-T-C

48782277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125444887-A-G

48782344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125444945-A-G

48782344-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125444945-A-T

http://identifiers.org/hco/15/GRCh38#48782382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125444985-C-A

48782382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125444985-C-T

48783290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125446539-T-C

48783291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125446540-G-T

48783326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125446571-A-G

http://identifiers.org/hco/15/GRCh38#48783958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125447241-C-A

http://identifiers.org/hco/15/GRCh38#48783968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125447251-C-A

48784039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125447322-T-C

48784039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125447322-T-G

48784043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125447326-A-G

http://identifiers.org/hco/15/GRCh38#48784243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125447497-C-A

http://identifiers.org/hco/15/GRCh38#48784544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125447728-A-C

http://identifiers.org/hco/15/GRCh38#48785011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125448189-C-A

48785011-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125448189-C-G

48785016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125448194-G-A

48785134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125448285-A-T

48785144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125448295-T-C

http://identifiers.org/hco/15/GRCh38#48785245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125448401-C-A

48785318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125448473-T-C

48785438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125448592-C-T

48785535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125448679-T-C

48786778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125450096-C-T

48786957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125450359-A-G

48786967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125450372-G-A

48786967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125450372-G-T

48787147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125450729-A-T

48787763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125451241-T-C

48788690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125452837-C-G

48788849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125452976-C-T

48788866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125452993-A-G

48788959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125453086-A-T

http://identifiers.org/hco/15/GRCh38#48789170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125453194-A-C

http://identifiers.org/hco/15/GRCh38#48789178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125453202-C-A

48789244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125453268-G-C

48789244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125453268-G-T

48789335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453336-G-A

48789335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453336-G-T

http://identifiers.org/hco/15/GRCh38#48789344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125453345-C-A

48789344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453345-C-T

48789403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453402-G-T

48789410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125453409-G-A

48791520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125455118-G-A

48791520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125455118-G-C

48791525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125455123-A-G

48792754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125455973-A-G

http://identifiers.org/hco/15/GRCh38#48793898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125456733-A-C

48795005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125458200-C-G

http://identifiers.org/hco/15/GRCh38#48795089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125458238-C-A

48795183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125458357-G-A

48795220-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125458394-A-T

48795858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125460028-T-C

48795858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125460028-T-G

http://identifiers.org/hco/15/GRCh38#48795859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125460029-C-A

48796080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125460363-T-C

http://identifiers.org/hco/15/GRCh38#48796134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125460417-C-A

48796134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125460417-C-T

48796147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125460430-T-G

http://identifiers.org/hco/15/GRCh38#48796153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125460436-C-A

48796162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 125460445-T-A

http://identifiers.org/hco/15/GRCh38#48796585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125460910-A-C

http://identifiers.org/hco/15/GRCh38#48796787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125461119-C-A

48796968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125461275-T-G

48797156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125461449-T-C

48797346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125461631-T-A

48797346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125461631-T-C

48797627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125461887-C-T

48797644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125461904-T-A

48797652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125461908-G-C

48797720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125461979-G-A

48797770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125462027-T-G

48797827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125462088-C-T

48797852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125462114-T-C

48797893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125462154-A-G

http://identifiers.org/hco/15/GRCh38#48797898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125462157-A-C

48797908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125462167-G-C

48797908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125462167-G-T

48797935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125462194-T-C

48797967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125462226-C-T

http://identifiers.org/hco/15/GRCh38#48798042-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125462301-A-C

48798084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125462343-A-T

48798362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125462600-A-G

48798518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125462711-G-A

48798527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125462720-G-A

48798540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125462731-C-T

48805426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125462970-G-T

http://identifiers.org/hco/15/GRCh38#48805463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125463012-C-A

48805463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125463012-C-T

http://identifiers.org/hco/15/GRCh38#48805497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125463046-C-A

48805497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125463046-C-G

48805497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125463046-C-T

48805527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125463066-T-C

http://identifiers.org/hco/15/GRCh38#48805554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125463084-A-C

48805554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125463084-A-G

48805554-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125463084-A-T

48805579-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125463109-T-A

48805579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125463109-T-C

48805664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 125463192-A-T

48810115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125466484-G-T

48810450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125466721-C-T

48810508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 125466772-A-G

48811005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 125466947-C-T

http://identifiers.org/hco/15/GRCh38#48811008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125466950-A-C

http://identifiers.org/hco/15/GRCh38#48811013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125466955-C-A

http://identifiers.org/hco/15/GRCh38#48811086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29298
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125467038-C-A