http://identifiers.org/hco/9/GRCh38#97412119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#45972326-C-A

97412119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45972326-C-T

97412176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: 5 prime UTR variant
orthologous variants: 45972374-C-G

97412176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: 5 prime UTR variant
orthologous variants: 45972374-C-T

97412226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 45972424-C-T

http://identifiers.org/hco/9/GRCh38#97412650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45972710-C-A

97412650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45972710-C-T

97412912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45972893-G-A

97413110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45973075-G-A

97413196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45973136-G-A

97413196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45973136-G-C

97413196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45973136-G-T

97413391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45973323-T-G

http://identifiers.org/hco/9/GRCh38#97414344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45974183-C-A

97414353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45974192-C-G

97414539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45975083-G-C

97414539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45975083-G-T

97415907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45979057-T-G

97416369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45979418-C-T

97416947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45979943-A-G

97417066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45980067-C-T

97417184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45980172-G-C

97417254-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45980236-G-T

97418175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45980498-C-T

97418352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45980653-G-A

97418463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45980784-G-A

97418463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45980784-G-T

97427835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45986961-C-T

97428087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45987162-C-T

97428323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45987323-G-A

97428398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45987402-A-G

97428420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45987424-A-G

97428525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 45987527-T-C

97428694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45987695-T-C

http://identifiers.org/hco/9/GRCh38#97430652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45988825-A-C

97430838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45989005-A-G

97430838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45989005-A-T

http://identifiers.org/hco/9/GRCh38#97430857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45989024-C-A

97430857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45989024-C-G

97430857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45989024-C-T

97430935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: 5_prime_UTR_variant, splice_region_variant, synonymous_variant
orthologous variants: 45989080-T-A

97430935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: 5_prime_UTR_variant, splice_region_variant, synonymous_variant
orthologous variants: 45989080-T-C

97431135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45989253-A-G

97431140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45989258-G-A

97431474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45989581-A-G

97431520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45989619-C-T

97431765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45989820-G-T

97432083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: synonymous variant
orthologous variants: 45990108-A-G

97432325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45990318-T-C

97432333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45990328-A-G

97432909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45990840-A-G

97433117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45991029-T-C

http://identifiers.org/hco/9/GRCh38#97438484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45991404-A-C

97438484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45991404-A-G

97438727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45991770-C-T

97438770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45991809-A-G

97438770-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45991809-A-T

97439101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45992092-A-T

97439272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: synonymous variant
orthologous variants: 45992224-A-G

97439307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: missense variant
orthologous variants: 45992259-A-T

97439314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: missense variant
orthologous variants: 45992266-G-T

http://identifiers.org/hco/9/GRCh38#97439329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45992281-C-A

97439329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45992281-C-T

http://identifiers.org/hco/9/GRCh38#97439357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45992298-C-A

http://identifiers.org/hco/9/GRCh38#97439371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45992312-C-A

97439371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45992312-C-T

http://identifiers.org/hco/9/GRCh38#97439372-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45992313-A-C

97439372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45992313-A-G

97439372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45992313-A-T

97439616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45992521-G-C

97439706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45992609-A-G

http://identifiers.org/hco/9/GRCh38#97439736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45992639-A-C

http://identifiers.org/hco/9/GRCh38#97439737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45992640-A-C

97439865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45992977-T-A

97439915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45993025-G-A

97439942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45993050-C-T

97439950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45993055-A-G

http://identifiers.org/hco/9/GRCh38#97441551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45994221-C-A

97441551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45994221-C-T

http://identifiers.org/hco/9/GRCh38#97441554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45994223-C-A

97441554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45994223-C-G

97441554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45994223-C-T

97441557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45994226-G-A

97441557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45994226-G-T

http://identifiers.org/hco/9/GRCh38#97441570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45994239-C-A

97441570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45994239-C-T

http://identifiers.org/hco/9/GRCh38#97441963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45994595-C-A

97441963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45994595-C-T

http://identifiers.org/hco/9/GRCh38#97441983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45994615-C-A

97441994-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45994631-T-A

http://identifiers.org/hco/9/GRCh38#97441996-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#45994633-A-C

97441996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45994633-A-G

97442988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45995423-G-A

97443017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45995437-C-T

97443353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45995768-A-G

97443439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45995849-A-T

97443843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45996105-C-G

97444185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45996420-C-T

97444792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45996965-T-C

97445080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45997341-C-G

97445477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45997831-A-G

97447242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45998983-G-A

97447470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45999161-C-G

97448208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45999784-C-G

97448208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 45999784-C-T

97448582-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46000115-T-A

97448663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46000203-A-G

97448737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46000280-T-C

97450065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46000771-G-A

http://identifiers.org/hco/9/GRCh38#97450158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46000864-C-A

97450158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46000864-C-G

97450313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46000973-G-A

97450564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46001172-G-A

97452322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46001796-T-C

97452366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46001839-T-C

97452643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46002121-A-G

97452674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46002135-T-C

97452709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46002162-C-T

97452822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46002417-A-G

97453177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46002701-A-G

97453239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46002765-C-T

97458880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46003673-T-C

97459472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46004496-G-A

97459639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46004608-A-G

97459733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46004706-T-C

97459734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46004707-G-T

97459835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46004812-T-G

97460101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46005043-T-C

97460158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46005097-G-A

97460435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 46005371-G-C

97460604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, missense_variant
orthologous variants: 46005540-G-A

97460667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, missense_variant
orthologous variants: 46005603-A-G

97460693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 46005629-A-G

97460723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 46005659-A-G

97460801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46005734-T-C

97460880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46005830-A-G

97463594-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46007059-C-G

97464693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46007363-A-G

97464693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46007363-A-T

http://identifiers.org/hco/9/GRCh38#97464821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46007434-C-A

97464821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46007434-C-T

http://identifiers.org/hco/9/GRCh38#97464826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46007439-C-A

97465166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46007748-A-G

97465403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46007961-A-G

97465404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46007962-A-G

97468902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46008678-A-G

97469084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46009082-C-T

97469136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46009132-C-T

97469188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46009176-A-G

97469447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46009385-G-C

97469622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46009525-G-A

97469622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46009525-G-T

97470291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, undefined
orthologous variants: 46010530-G-T

http://identifiers.org/hco/9/GRCh38#97470453-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46010679-A-C

97470453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46010679-A-G

http://identifiers.org/hco/9/GRCh38#97470457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46010683-A-C

http://identifiers.org/hco/9/GRCh38#97470468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46010694-C-A

97470468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46010694-C-T

97470475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46010701-T-G

97470518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46010739-G-A

97470518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46010739-G-C

97470638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 46010870-C-G

http://identifiers.org/hco/9/GRCh38#97470692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46010922-C-A

97470692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46010922-C-T

97471421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46012159-G-T

97471460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46012195-G-A

97471539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46012272-T-C

97471744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46012461-G-T

97471979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46012702-T-C

97472076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46012793-C-T

http://identifiers.org/hco/9/GRCh38#97472179-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46012961-A-C

97472185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46012967-G-T

http://identifiers.org/hco/9/GRCh38#97472218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46012997-C-A

97472226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46013003-A-G

97472226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46013003-A-T

97472231-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46013008-T-G

97472235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46013012-T-A

97472235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46013012-T-G

97472238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46013015-A-G

97472280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46013053-C-G

97472312-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 46013085-T-A

97472312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 46013085-T-C

97472327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 46013100-G-A

97472348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 46013121-T-C

97472613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46014302-G-A

97472613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46014302-G-T

97472631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46014320-G-A

97472631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46014320-G-T

97472632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46014321-G-A

97472632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46014321-G-T

97473620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: synonymous variant
orthologous variants: 46016997-T-C

97473856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46017207-A-G

97473873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46017227-A-T

97474262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46017500-A-G

97474647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46017839-A-G

97474678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46017898-C-T

97474841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46018058-A-G

97475030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46018190-G-A

97475030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46018190-G-T

97475283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46018440-G-A

97475283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46018440-G-C

97475283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46018440-G-T

http://identifiers.org/hco/9/GRCh38#97475287-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46018444-A-C

97475346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46018493-A-G

97475550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46018692-T-C

97475550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46018692-T-G

http://identifiers.org/hco/9/GRCh38#97475573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46018713-C-A

97475573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46018713-C-T

97476829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46019668-A-G

97477397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46020123-C-T

97478329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46020725-T-G

97478471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: missense variant
orthologous variants: 46020837-T-A

97478706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46021007-T-C

97478850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46021146-G-A

97478927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46021230-G-A

97478943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46021245-G-C

97478945-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46021247-A-T

97479241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46021943-A-G

97479283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46021974-A-G

97479311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022001-G-A

97479311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022001-G-C

97479352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022062-G-C

97479633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022329-C-G

97479771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022439-G-A

97479917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022614-C-T

97479955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022654-C-G

97480044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022721-A-G

http://identifiers.org/hco/9/GRCh38#97480126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46022797-C-A

97480126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022797-C-T

97480147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022817-G-A

97480247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022896-G-A

97480247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022896-G-C

97480247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022896-G-T

http://identifiers.org/hco/9/GRCh38#97480270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46022926-A-C

97480270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022926-A-G

97480286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46022942-G-A

97480376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 46023021-G-A

97480548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 46023157-G-T

97480628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 46023224-G-A

97480632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 46023228-A-G

http://identifiers.org/hco/9/GRCh38#97480634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46023230-A-C

97480634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 46023230-A-G

97480652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 46023247-A-G

97480691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 46023283-G-A

97480948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46023515-C-G

97480948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46023515-C-T

97481351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46023837-T-C

97481986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46024988-T-C

97482101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46025094-G-C

97482858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 46025666-G-A

97483103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: missense variant
orthologous variants: 46025911-G-A

97483298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: synonymous variant
orthologous variants: 46026106-G-A

97483726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46026622-A-G

97484312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46027059-C-G

97484312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46027059-C-T

97484678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46027390-A-G

97485149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46027791-G-A

97485245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46027879-G-A

97485496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46028111-A-G

97485627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46028236-C-T

http://identifiers.org/hco/9/GRCh38#97485679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46028269-A-C

97485987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46028564-C-T

97486638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46028813-C-T

97486897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46029051-G-A

97487122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46029599-G-A

97487156-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46029631-T-A

97487274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: missense variant
orthologous variants: 46029749-G-C

97487408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46029879-T-G

http://identifiers.org/hco/9/GRCh38#97487474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46029939-C-A

97487474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46029939-C-T

97487537-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46029979-T-G

97487685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46030159-T-C

97488002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46030445-A-G

97488021-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46030448-T-G

97488261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46030694-G-A

97488262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46030695-C-G

97488293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46030727-A-G

97488295-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46030729-A-G

97488321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46030749-G-A

97488345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46030764-G-A

97488350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46030769-T-C

97488570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46030975-T-G

97488744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46031122-G-A

97488760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46031167-T-C

http://identifiers.org/hco/9/GRCh38#97488830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#46031230-A-C

97488847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46031251-G-A

97495419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46034072-A-G

97495567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: intron variant
orthologous variants: 46034202-A-T

97495817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: synonymous variant
orthologous variants: 46034450-A-G

97496093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30831
most severe consequence: 3 prime UTR variant
orthologous variants: 46034730-A-G