106861752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54946654-G-C

106861752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54946654-G-T

106861803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54946712-T-G

106863024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54947883-A-G

106863836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54948776-G-A

106864042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54948983-C-G

106864059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54949000-T-C

106864059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54949000-T-G

106864113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54949043-T-A

106864113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54949043-T-C

106864151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54949082-G-C

106864226-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54949147-T-G

106864267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54949187-G-C

http://identifiers.org/hco/9/GRCh38#106864376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54949289-C-A

106864768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54949734-C-T

106865461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54950443-G-A

106867226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54952284-A-G

106867226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54952284-A-T

http://identifiers.org/hco/9/GRCh38#106867497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54952476-A-C

106867536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54952518-T-C

106867626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54952602-C-G

106867626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54952602-C-T

http://identifiers.org/hco/9/GRCh38#106868053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54953105-A-C

106868093-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54953150-T-A

106868093-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54953150-T-G

106868465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54953519-G-T

106868466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54953520-G-A

106868584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54953643-C-T

106868644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54953718-T-C

106868877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54953930-A-G

106868906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54953960-T-C

106868955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54954005-A-G

106868982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54954020-T-C

106869373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54954423-C-T

106869703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54954724-G-A

106870289-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54955263-C-G

106870400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54955382-T-C

106870627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54955600-A-G

106870879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54955851-C-G

106870879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54955851-C-T

106871256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54956294-C-T

106871288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54956327-G-A

106871300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54956339-G-A

106871515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54956537-A-G

106871994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54957036-C-T

106872333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54957409-G-C

106872867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54957591-T-A

106872901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54957622-T-C

http://identifiers.org/hco/9/GRCh38#106873073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54957787-C-A

106873223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54957917-A-G

106873276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54957966-C-T

106873296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54957977-T-C

106873298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54957979-G-A

106873309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54957990-C-T

106873482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54958253-G-A

106873482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54958253-G-T

106873518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54958279-A-G

106873534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54958295-C-T

106873564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54958320-T-C

106873590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54958343-A-G

106873595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54958348-C-G

106873595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54958348-C-T

106873870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54958614-T-C

106873973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54958712-C-T

106874104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54958932-T-A

http://identifiers.org/hco/9/GRCh38#106874522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54959362-A-C

106874593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54959443-A-G

106874666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54959525-G-A

http://identifiers.org/hco/9/GRCh38#106874726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54959579-C-A

106874726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54959579-C-G

106874726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54959579-C-T

106874727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54959580-G-A

106874727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54959580-G-T

106874735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54959588-G-A

106874735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54959588-G-C

106874739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54959592-C-G

106875451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54960274-T-C

106875824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54960997-A-G

106875932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54961100-A-G

106875985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54961148-A-G

106876278-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54961488-G-C

106876391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54961750-C-T

106876400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54961759-G-T

106876701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54962177-G-A

106877006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54962463-A-G

106877042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54962498-G-A

http://identifiers.org/hco/9/GRCh38#106877966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54965064-C-A

106878232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54965301-G-A

106878602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54965668-C-T

106879796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54966873-T-C

106880129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54967183-A-G

106880221-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54967274-T-G

106880467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54967395-C-T

106880660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54967582-G-T

106880732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54967654-A-G

106880792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54967714-T-G

http://identifiers.org/hco/9/GRCh38#106880805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54967727-A-C

106880909-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54967831-T-G

106880953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54967871-G-A

106881064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54967980-G-T

106881321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54968218-A-G

106881527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54968421-C-T

106881703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54968594-G-A

106881789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54968654-C-T

http://identifiers.org/hco/9/GRCh38#106881800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54968661-C-A

106881988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54968842-G-A

106882056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54968912-C-T

106882134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54968989-A-G

106882195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54969052-T-C

106882496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54969171-T-C

106882497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54969172-A-G

http://identifiers.org/hco/9/GRCh38#106882958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54969615-A-C

106883058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54969707-T-C

106883152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54969801-A-T

106883381-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54970030-C-G

106883801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54970462-C-T

106883813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54970474-C-T

106883814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54970475-G-A

106884044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54970808-C-T

http://identifiers.org/hco/9/GRCh38#106884390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54971100-C-A

106884390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54971100-C-T

106884491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54971165-G-A

106884974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54971642-A-T

106885120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54971779-C-T

106885293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54971940-A-G

106885529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54972157-C-T

106885656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54972284-G-A

http://identifiers.org/hco/9/GRCh38#106885665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54972293-A-C

106885746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54972374-A-G

106885869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54972497-T-A

106886036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54972665-A-G

106886056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54972685-A-G

106886095-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54972722-A-T

106886143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54972770-A-G

106886195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54972819-A-G

106886459-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54973077-G-C

106886523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54973141-C-T

106886720-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54973341-T-G

106886951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54973569-C-T

106886996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54973599-T-A

106887357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54973924-A-G

106887392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54974128-G-C

106887944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54974675-T-C

106888015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54974744-A-G

106888047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54974776-T-A

106888603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54975031-C-T

106888768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54975453-G-A

106888791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54975515-T-A

106888833-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54975607-C-T

106889008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54975946-T-C

106889217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54976149-A-G

106889217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54976149-A-T

106889343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54976276-G-C

106889372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54976305-G-T

106889468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54976398-T-C

106889604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54976528-C-T

106889677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54976694-G-T

106889691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54976708-G-T

http://identifiers.org/hco/9/GRCh38#106889784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54976793-C-A

106889944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54976938-T-C

106890143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54977132-A-G

106890438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54977376-A-G

106890605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54977680-G-C

106890616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54977691-G-A

106890826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54977892-C-G

106890860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54977925-G-C

106891017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54978052-A-G

106891429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54978510-G-C

106891600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54978678-G-C

106891698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54978774-A-G

106891797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54978884-A-T

106891998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54979119-C-G

106891998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54979119-C-T

106892192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54979299-A-G

106892400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54979516-T-A

106892400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54979516-T-C

106892529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54979638-C-T

106893147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 54980234-T-G

106893353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54980437-G-C

106893394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54980478-A-G

106893525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54980605-A-T

106893710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54981151-T-A

106893710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54981151-T-C

106893789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54981254-G-A

106893959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54981417-A-G

106894007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54981449-C-G

http://identifiers.org/hco/9/GRCh38#106894167-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54981649-A-C

106894274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54981837-G-A

106894364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54981928-C-T

106894408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54981969-A-G

106894474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54982027-T-G

106894515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54982068-A-G

106894629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54982177-G-C

http://identifiers.org/hco/9/GRCh38#106894996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54982494-C-A

106894996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54982494-C-T

106895004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54982513-G-A

106895228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54982670-T-C

106895276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54982717-T-C

106895474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54982918-C-T

106895632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54983070-G-A

106895632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54983070-G-T

106895638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54983076-T-G

106895719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54983179-C-G

106895719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54983179-C-T

106896024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54983848-T-C

106896233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54984050-A-G

106896343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54984152-T-A

106896418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54984245-A-G

106896578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54984408-G-A

106896639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54984471-G-A

http://identifiers.org/hco/9/GRCh38#106896936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54984758-C-A

106896937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54984759-C-T

http://identifiers.org/hco/9/GRCh38#106896981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54984794-A-C

106896981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54984794-A-G

106897183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54985024-T-G

106897191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54985032-A-G

106897595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54985355-A-G

106898363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54985982-A-G

106898390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54986023-T-C

106898581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54986199-A-G

106898763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54986380-A-G

106898875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54986461-G-A

106898971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54986549-A-G

106899520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54986881-G-A

106899556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54986920-A-G

106899650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54986992-A-G

106906479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54987184-G-A

106906479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54987184-G-T

http://identifiers.org/hco/9/GRCh38#106906537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54987238-A-C

106906728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54987392-A-G

106906768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54987424-T-C

106906776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54987432-A-G

http://identifiers.org/hco/9/GRCh38#106907268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54988175-A-C

http://identifiers.org/hco/9/GRCh38#106907305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54988213-C-A

106907705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54988748-G-A

106907928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54989185-A-G

106907931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54989188-G-A

106907993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54989248-A-T

106908001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54989256-G-A

106908121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54989381-A-G

106908180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54989444-T-C

106908193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54989457-C-G

106908500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54989764-T-C

106909952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54990537-C-T

106910331-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54990907-A-T

106910699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54991200-G-T

106910736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54991221-T-C

106910801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54991280-A-G

106910919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54991416-T-G

106911041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54991534-T-C

106911140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54991615-G-A

106911142-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54991617-A-T

106911377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54992280-T-C

106911389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54992299-C-T

106911428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54992334-T-G

106911618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54992469-G-A

106911990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54993579-C-T

106912175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54993757-C-T

106912239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54993821-A-G

106912370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54993942-T-G

106912826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54994355-A-G

106912878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54994395-A-G

106912893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54994411-A-G

106912896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54994414-C-G

106912964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54994478-A-G

106913011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54996937-A-G

106913024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54996950-G-A

106913044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54996959-G-C

106913100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54997046-T-C

106913147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54997162-G-C

106913149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54997164-C-G

106913196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 54997230-G-A

106913946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54997691-C-T

106914148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54997850-T-C

106914420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54998131-T-C

106914450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54998160-G-A

106914493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54998202-T-C

106914739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54998519-C-G

106914966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54998701-A-T

http://identifiers.org/hco/9/GRCh38#106915134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#54998858-A-C

106915360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54999163-T-C

106915436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 54999241-T-G

http://identifiers.org/hco/9/GRCh38#106916031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55000577-C-A

106916235-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55000775-A-T

106916271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55000811-C-G

106916271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55000811-C-T

106916572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55001115-G-A

106916572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55001115-G-C

106916572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55001115-G-T

106916753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 55001297-G-A

http://identifiers.org/hco/9/GRCh38#106916861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55001410-C-A

106917113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, undefined
orthologous variants: 55001658-A-G

106917161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, undefined
orthologous variants: 55001704-T-G

106917256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, undefined
orthologous variants: 55001806-G-A

106917256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, undefined
orthologous variants: 55001806-G-T

106917409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55001958-T-C

106917416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55001965-A-T

106917468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55002017-A-G

106917798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55002349-T-C

106918255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55002411-C-T

106918468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55002634-G-A

106918499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55002665-A-T

106918534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55002699-A-G

106918670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55002831-T-C

106918883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55003043-T-G

106918993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55003154-G-A

106919005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55003166-A-G

106919051-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55003212-A-T

106919585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55003731-T-C

106919745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55003880-T-C

106919998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55004148-A-T

106920025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55004172-T-A

106920025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55004172-T-C

106920087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55004233-C-G

106920158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55004315-C-T

106920723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55004894-T-G

106920751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55004922-A-G

106921048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55005213-G-A

106921048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55005213-G-C

106921234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55005402-C-T

106921337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55005506-G-C

106921413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55005582-C-T

106921959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55006132-G-A

106922482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55006679-T-A

106922508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55006705-G-A

106922728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55006927-G-C

106922729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55006928-G-A

106922730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55006929-A-G

106922946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55007136-G-A

106922946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55007136-G-T

106922967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55007157-G-A

106923243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55007429-G-T

http://identifiers.org/hco/9/GRCh38#106923317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55007496-C-A

106923317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55007496-C-T

106923342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55007521-C-T

106923470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: synonymous variant
orthologous variants: 55007649-A-G

106923476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: synonymous variant
orthologous variants: 55007655-G-A

106923476-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: synonymous variant
orthologous variants: 55007655-G-C

http://identifiers.org/hco/9/GRCh38#106923631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55007809-C-A

106923631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55007809-C-T

106923650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55007838-T-A

http://identifiers.org/hco/9/GRCh38#106923671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55007860-C-A

106923982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55008098-T-C

106923982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55008098-T-G

106924010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55008123-G-C

106924010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55008123-G-T

106924092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron variant
orthologous variants: 55008204-T-G

106924149-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: synonymous variant
orthologous variants: 55008272-A-T

http://identifiers.org/hco/9/GRCh38#106924158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55008281-C-A

106924158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: synonymous variant
orthologous variants: 55008281-C-T

106924656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55008779-C-T

106924770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55008890-T-C

106924775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant
orthologous variants: 55008895-T-A

106924775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant
orthologous variants: 55008895-T-G

106925003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant
orthologous variants: 55009129-G-A

106925003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant
orthologous variants: 55009129-G-C

106925034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55009160-T-C

106925034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55009160-T-G

http://identifiers.org/hco/9/GRCh38#106925136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55009262-A-C

106925547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55009670-A-G

106925553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55009676-A-G

http://identifiers.org/hco/9/GRCh38#106925571-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55009694-A-C

106925571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55009694-A-G

http://identifiers.org/hco/9/GRCh38#106925706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55009808-C-A

106925706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55009808-C-T

106925973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55010075-G-A

106926171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55010273-T-G

http://identifiers.org/hco/9/GRCh38#106926174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55010276-C-A

106926174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55010276-C-T

106926204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55010306-T-C

106926315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55010417-T-C

106926561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55010660-T-C

106926780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55010879-G-A

106926801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55010900-C-G

106926801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 55010900-C-T

106927491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55011584-C-T

http://identifiers.org/hco/9/GRCh38#106927629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55011722-A-C

http://identifiers.org/hco/9/GRCh38#106927699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55011789-C-A

106927699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 55011789-C-T

106928081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55012171-C-G

106928081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55012171-C-T

106928211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55012301-A-G

106928382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55012472-G-A

106928382-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55012472-G-C

106928577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55012667-T-C

106928706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55012796-G-T

106928925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55013015-G-A

http://identifiers.org/hco/9/GRCh38#106929039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55013129-C-A

http://identifiers.org/hco/9/GRCh38#106929147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55013237-C-A

106929147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55013237-C-G

106929147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55013237-C-T

106929370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55013460-C-T

106929384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55013474-G-A

106929413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55013503-T-C

106929413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55013503-T-G

106929627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55013717-C-T

106929913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55014000-T-C

106929941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55014028-C-G

106930215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55014402-G-A

106930216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55014403-C-T

106930243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55014430-G-C

106930272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55014459-T-C

106930377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55014550-T-C

106930429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55014587-G-A

106930429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55014587-G-T

http://identifiers.org/hco/9/GRCh38#106930431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55014589-C-A

106930791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55015005-G-A

106930864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55015078-T-C

106930936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55015145-A-G

106930973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55015183-A-G

106931076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55015268-C-T

106931187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55015388-C-T

106931941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55016501-G-C

106932110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55016662-C-T

106932117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55016669-G-A

106932596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55017146-A-G

106932710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55017246-G-A

106932710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55017246-G-T

106932788-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55017320-G-C

106932845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55017373-T-A

106932845-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55017373-T-G

http://identifiers.org/hco/9/GRCh38#106933030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55017727-C-A

106933348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55017973-G-C

106933750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55018319-G-A

106934022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55018589-G-C

106934324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55018857-G-C

106934324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55018857-G-T

106934877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55019250-G-T

106934880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55019253-T-C

106934884-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55019257-T-A

106934975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55019351-A-G

106935036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55019406-G-A

106935068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55019437-G-C

106935092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55019454-C-T

106935105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55019492-T-A

http://identifiers.org/hco/9/GRCh38#106935208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55019634-C-A

http://identifiers.org/hco/9/GRCh38#106935282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55019873-C-A

http://identifiers.org/hco/9/GRCh38#106935404-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55020006-C-A

106935404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55020006-C-T

106935457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55020053-A-G

106935578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55020164-C-G

106935658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55020237-A-G

106935658-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55020237-A-T

http://identifiers.org/hco/9/GRCh38#106935659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55020238-C-A

106935659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55020238-C-T

106935791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55020349-G-A

106936282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55020684-T-C

106936287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55020689-T-C

106936418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55020790-C-T

http://identifiers.org/hco/9/GRCh38#106936617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55020971-C-A

106936649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55021003-G-C

106936950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55021292-G-T

106937008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55021350-G-A

106937856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55022056-T-C

106938137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55022615-G-T

106938323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55022865-T-C

106938378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55022918-T-A

106938450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55023010-A-G

106938588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55023113-G-C

106938686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55023193-A-G

106938786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55023289-G-A

106938786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55023289-G-T

106938983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55023482-C-G

106938983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55023482-C-T

106939118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55023617-G-A

106939118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55023617-G-T

http://identifiers.org/hco/9/GRCh38#106939138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55023637-C-A

106939138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55023637-C-T

106939169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55023668-G-A

http://identifiers.org/hco/9/GRCh38#106939171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55023670-C-A

106939387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55023850-C-G

106939387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55023850-C-T

106940110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55024491-G-A

106940110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55024491-G-T

106940347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55024719-A-G

106940366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55024737-G-A

http://identifiers.org/hco/9/GRCh38#106940392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55024763-C-A

106940392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55024763-C-T

106940731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55025009-A-G

106941751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55026038-T-A

106941864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55026143-G-A

106942428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55026723-T-C

106942487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55026774-G-A

106942491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55026779-C-G

106942491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55026779-C-T

http://identifiers.org/hco/9/GRCh38#106942561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55026849-A-C

106942561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55026849-A-G

106942981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55027214-T-C

106943270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55027623-A-G

106943335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55027685-C-T

106943680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55028037-A-G

106943748-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55028094-A-T

106943858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55028207-T-C

106944059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55028407-G-A

106944181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55028508-G-A

106945123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55028736-A-G

106945280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55028847-G-C

106945368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55028934-G-T

106945578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55029157-G-A

106945880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55029449-A-G

106945922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55029488-G-A

106945997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55029606-G-A

106945997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55029606-G-T

106946090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55029705-C-G

106946345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55029958-C-G

106946510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55030105-T-C

106946510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55030105-T-G

106946585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55030179-A-G

106946641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55030207-G-A

106946906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55030253-A-T

106947032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55030379-G-A

106947080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55030431-G-A

106947082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55030433-G-A

106947467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55030797-A-G

106947771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55031106-C-G

106947829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55031163-C-G

106948184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55031436-G-A

106948291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55031525-A-G

106948337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55031574-C-T

106948684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55032010-G-T

106948766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55032095-C-T

106948776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55032105-T-C

http://identifiers.org/hco/9/GRCh38#106949200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55032540-A-C

106949200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55032540-A-G

106949213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55032553-A-G

http://identifiers.org/hco/9/GRCh38#106949418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55032813-A-C

106949418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55032813-A-G

106949654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55033117-C-T

106949717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55033182-G-A

106949824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55033285-T-C

106950044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55033509-T-A

106950123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55033962-T-G

106950269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55034108-C-G

106950273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55034112-G-A

106950352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55034176-G-A

106951108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55034843-G-T

106951360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55035015-G-C

106952259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55035786-C-T

106952552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55036126-G-C

106952564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55036138-T-C

106952631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55036199-T-G

106953103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55036840-T-C

106953131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55036863-C-T

106953141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55036873-A-G

106953295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55037007-C-G

106953456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55037097-T-G

106953542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55037201-C-G

106953775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55037401-C-T

106954939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55037977-A-G

106954984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55038019-G-A

106957894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55038232-T-G

106957962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55038300-A-G

106958359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55038639-A-T

106958684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55038916-C-T

106958847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55039001-C-T

106958975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55039117-C-T

106959012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55039154-A-G

106959015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55039161-G-A

106959015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55039161-G-C

106959031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55039177-G-C

http://identifiers.org/hco/9/GRCh38#106959217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55039341-C-A

106959275-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55039399-A-T

106959311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55039435-A-G

106959397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55039555-A-G

106960138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55040329-A-G

106960185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55040372-G-A

http://identifiers.org/hco/9/GRCh38#106960295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55040474-C-A

106960389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55040569-C-T

106960777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55040978-T-C

106960790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55040991-A-G

http://identifiers.org/hco/9/GRCh38#106961033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55041211-C-A

106961733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55041849-C-G

106961736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55041852-A-G

106961776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55041892-G-A

106962074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55042073-A-G

106962089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55042088-A-G

106962632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55042577-A-G

106962780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55042729-G-A

106962869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55042818-C-T

106963049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55043000-G-A

106963049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55043000-G-T

106963253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55043174-C-T

106963671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55043904-A-G

http://identifiers.org/hco/9/GRCh38#106965952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55044939-C-A

106965974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55044953-C-T

106966172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55045125-T-C

106966309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55045840-T-C

106966331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55045859-G-T

106966687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55046217-G-A

106966695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55046225-A-G

106966719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55046249-T-C

106966767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55046285-C-G

106967008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55046507-G-A

106967116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55046586-A-T

106967354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55046819-T-C

106967392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55046865-G-C

106967436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55046904-C-T

106967505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55046983-G-A

106968888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55047297-C-T

106968942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55047345-A-G

106969246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55047607-A-G

106969499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55047863-C-T

106969547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55047915-G-A

106969579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55047940-C-T

106969839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55048147-G-C

106969942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55048221-G-A

106970148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55048417-A-G

106970190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55048461-C-T

106970449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55048671-C-T

106970576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55048802-C-T

106970693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55048906-T-C

http://identifiers.org/hco/9/GRCh38#106970697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55048910-C-A

http://identifiers.org/hco/9/GRCh38#106970803-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55048993-C-A

106970877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55048998-T-A

106971192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55049298-C-T

106971282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55049392-G-A

106971320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55049432-G-A

http://identifiers.org/hco/9/GRCh38#106971353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#55049465-C-A

106971883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55050025-G-A

106971883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55050025-G-C

106972144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55050325-C-T

106972145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55050326-G-A

106972145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 55050326-G-T

http://identifiers.org/hco/9/GRCh38#106972290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55050471-C-A

106972296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55050477-T-C

106972297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55050478-G-A

http://identifiers.org/hco/9/GRCh38#106972330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55050512-C-A

106972330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55050512-C-T

106972523-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55050699-T-G

http://identifiers.org/hco/9/GRCh38#106973905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55050989-C-A

106973923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55051008-T-C

106973923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55051008-T-G

http://identifiers.org/hco/9/GRCh38#106973997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55051075-C-A

http://identifiers.org/hco/9/GRCh38#106974058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55051129-C-A

106974058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55051129-C-T

106974176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 55051230-A-G

106974297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55051354-T-C

106974345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55051435-C-G

106974345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 55051435-C-T

106974356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 55051446-G-A

106974368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55051455-G-A

106974369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55051456-T-C

106974538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55051589-T-C

106974575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55051615-G-A

106974575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55051615-G-T

http://identifiers.org/hco/9/GRCh38#106974609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55051646-A-C

106974609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55051646-A-G

106974612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55051648-G-A

106974612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55051648-G-T

106974881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55051821-A-G

http://identifiers.org/hco/9/GRCh38#106974942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55051873-C-A

106974973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55051904-A-G

106975002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052044-G-T

106975066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052147-G-T

106975148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052225-A-G

106975171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052248-G-A

http://identifiers.org/hco/9/GRCh38#106975295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55052377-C-A

106975311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052391-G-A

106975388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052500-T-C

106975461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052569-G-A

106975461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052569-G-T

http://identifiers.org/hco/9/GRCh38#106975498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55052603-C-A

106975502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052607-G-A

106975502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052607-G-T

106975534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052642-T-C

106975536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052644-G-T

106975540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052648-G-T

106975653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052762-A-G

106975873-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55052993-A-T

http://identifiers.org/hco/9/GRCh38#106975906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55053008-C-A

106975906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55053008-C-T

106976158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55053307-A-T

106976237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55053399-C-T

106976287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55053432-A-G

106976314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55053460-A-G

http://identifiers.org/hco/9/GRCh38#106976480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55053695-C-A

106976480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55053695-C-T

106976544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55053799-T-C

106976697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55053941-C-T

106976795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55054003-T-C

106976807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55054015-A-G

106976824-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55054034-T-A

106976827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55054037-C-G

106977020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55054229-G-A

106977040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55054249-T-C

106977284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55054468-C-T

106977553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55054737-A-G

106977590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55054774-C-T

106977954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55055147-C-G

106978069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55055269-G-A

http://identifiers.org/hco/9/GRCh38#106978175-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55055370-A-C

106978175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55055370-A-G

106978291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55055485-C-T

http://identifiers.org/hco/9/GRCh38#106978542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55055696-A-C

106979601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55055830-G-A

106979601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55055830-G-T

http://identifiers.org/hco/9/GRCh38#106979759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55055957-C-A

106979798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55055991-A-G

106980222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55056378-G-T

106980767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 55057105-A-G

106981754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55057667-A-G

106981806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55057720-T-A

106981879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55057793-C-T

106981937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55057850-G-C

106982423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55058284-A-G

106982475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55058338-T-A

106982475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55058338-T-C

106982498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55058359-G-T

http://identifiers.org/hco/9/GRCh38#106982537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55058401-A-C

106982850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55058715-G-A

http://identifiers.org/hco/9/GRCh38#106982917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55058780-C-A

106983304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55059161-C-T

106983359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55059220-G-A

106983469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55059296-G-T

106983529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55059353-G-C

106984034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55059902-G-T

106984114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55059943-T-C

106984123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55059952-G-A

106984134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55059963-T-C

106984334-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55060162-T-G

106984417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55060246-C-T

http://identifiers.org/hco/9/GRCh38#106984423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55060252-C-A

106984423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55060252-C-T

106984426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55060255-C-T

http://identifiers.org/hco/9/GRCh38#106984446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55060296-C-A

106984468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55060305-G-A

106984676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55060454-A-G

106985344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55060868-G-A

106985348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55060872-G-T

106985477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55060969-C-T

106985785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55061256-G-A

106985923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55061356-C-G

106986075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55061500-A-G

106986080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55061505-G-A

106986231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55061656-C-G

106986592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55062015-T-G

http://identifiers.org/hco/9/GRCh38#106992935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55065153-A-C

106992996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065195-G-T

106992999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065198-A-G

106993167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065376-G-C

106993337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065541-G-A

106993583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065785-T-C

106993657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065814-C-T

http://identifiers.org/hco/9/GRCh38#106993674-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55065825-A-C

106993674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065825-A-G

106993975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065958-A-G

106993988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55065971-C-G

106994583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55066556-G-C

106994598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55066571-T-C

106994714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55066689-G-A

106994926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55066876-A-G

106995095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55067026-G-A

106995215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55067136-G-A

106995473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55067390-C-T

106995476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55067393-T-C

http://identifiers.org/hco/9/GRCh38#106995545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55067468-C-A

106995612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55067531-A-G

106995612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55067531-A-T

106995631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55067550-G-A

106995752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55067681-G-A

http://identifiers.org/hco/9/GRCh38#106998001-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55068740-A-C

106998091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55068814-T-C

106998101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55068824-A-G

106998236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55069035-G-T

106998769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55069347-T-C

106998933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55069613-G-A

106999218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55069879-A-G

106999245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55069906-T-C

106999287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55069949-G-A

106999341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55070016-A-G

107000049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55070478-G-A

107000096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55070524-G-C

107000821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55071451-G-T

107001888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55071554-G-A

107001998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55071648-A-G

http://identifiers.org/hco/9/GRCh38#107002288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55071914-C-A

107002339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55071966-G-A

107002602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55072186-C-T

http://identifiers.org/hco/9/GRCh38#107002620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55072204-A-C

107002913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55072624-A-G

107002934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55072651-A-G

107003230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55072914-C-T

107003263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55072942-T-C

107003308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55072987-T-C

107003519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55073200-G-A

107003546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55073227-G-T

107003669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55073351-T-C

107004818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55074555-G-A

107005114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55074866-A-G

107005502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075211-A-T

107005539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075278-T-C

107005652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075387-T-C

107005653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075388-G-A

107005721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075458-C-T

107005870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55075618-G-A

107006482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55076149-G-A

107006509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55076177-C-T

107006678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55076291-C-G

107006772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55076360-A-T

107007288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55076904-G-A

107007289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55076905-T-C

107008479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078028-G-A

107008591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078126-A-G

107008892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078428-A-G

107008901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078437-G-T

107009119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55078834-A-G

107009191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55078904-G-C

107009228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55078939-A-G

107009420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55079132-G-A

107009457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55079176-A-T

107009523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55079238-C-T

107009537-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55079256-C-G

107009537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55079256-C-T

107009663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 55079382-C-T

http://identifiers.org/hco/9/GRCh38#107009745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55079448-C-A

107009791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55079505-G-T

107009921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55079596-A-G

http://identifiers.org/hco/9/GRCh38#107009988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55079650-C-A

107009988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55079650-C-T

http://identifiers.org/hco/9/GRCh38#107010001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55079663-C-A

107010364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55079976-C-T

107010394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55080011-T-A

107010431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55080048-T-C

107010463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55080081-G-A

107010463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55080081-G-C

107010571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55080140-A-G

107010676-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55080232-A-T

http://identifiers.org/hco/9/GRCh38#107010681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55080237-C-A

107010681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55080237-C-T

107010745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55080470-G-A

107010745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55080470-G-T

107010755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55080480-A-T

http://identifiers.org/hco/9/GRCh38#107010786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55080535-C-A

http://identifiers.org/hco/9/GRCh38#107010796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55080642-C-A

107010796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55080642-C-T

107010806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55080652-G-A

107010806-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55080652-G-C

107010824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55080667-G-A

107010824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55080667-G-C

107010824-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55080667-G-T

107010993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55080836-A-G

http://identifiers.org/hco/9/GRCh38#107011987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55081842-A-C

107012153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082031-T-A

107012153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082031-T-C

http://identifiers.org/hco/9/GRCh38#107012154-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55082032-C-A

107012154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082032-C-G

107012154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082032-C-T

107012161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082039-G-T

http://identifiers.org/hco/9/GRCh38#107012196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55082074-C-A

107012421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082284-G-A

107012421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082284-G-T

http://identifiers.org/hco/9/GRCh38#107012435-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55082298-C-A

107012435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082298-C-T

107012472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082300-G-T

http://identifiers.org/hco/9/GRCh38#107012480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#55082308-C-A

107012480-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082308-C-G

107012480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082308-C-T

107012625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082463-G-T

107012655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082495-G-A

107012666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082506-A-T

107012955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55082872-G-A

107013119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55083021-G-A

107013119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21684
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 55083021-G-T