21217330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692451-T-C

http://identifiers.org/hco/1/GRCh38#21217421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137692351-C-A

21217455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692324-G-A

21217477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692287-T-A

21217477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692287-T-C

http://identifiers.org/hco/1/GRCh38#21217508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137692258-C-A

21217508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692258-C-G

21217508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692258-C-T

http://identifiers.org/hco/1/GRCh38#21217544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137692245-C-A

21217544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692245-C-T

21217570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692222-G-T

http://identifiers.org/hco/1/GRCh38#21217578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137692219-C-A

21217578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692219-C-T

21217650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692177-A-G

21217658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692170-A-G

21217662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692166-T-A

21217662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692166-T-G

http://identifiers.org/hco/1/GRCh38#21217663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137692165-C-A

21217663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692165-C-G

21217663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692165-C-T

21217680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692148-A-G

21217680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692148-A-T

21217692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692139-G-A

21217692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3 prime UTR variant
orthologous variants: 137692139-G-T

21217742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 137692089-G-A

21217742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 137692089-G-T

http://identifiers.org/hco/1/GRCh38#21217752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137692087-C-A

21217752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 137692087-C-T

http://identifiers.org/hco/1/GRCh38#21217790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137692047-C-A

21217790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 137692047-C-T

21217874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 137691988-G-T

21217875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 137691987-G-T

21217880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 137691982-T-C

21217885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 137691973-G-A

21217885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 137691973-G-T

21217887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 137691971-G-A

21217887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 137691971-G-T

21217916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 137691942-T-C

21217938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 137691866-G-A

21217938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 137691866-G-T

http://identifiers.org/hco/1/GRCh38#21217941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137691863-C-A

21217950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 137691861-G-A

21217950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 137691861-G-T

http://identifiers.org/hco/1/GRCh38#21217952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137691859-C-A

21217952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 137691859-C-T

http://identifiers.org/hco/1/GRCh38#21218051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137691766-C-A

21218051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691766-C-T

http://identifiers.org/hco/1/GRCh38#21218091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137691728-C-A

21218091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 137691728-C-T

21218134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691685-A-G

http://identifiers.org/hco/1/GRCh38#21218233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137691547-C-A

21218233-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691547-C-G

http://identifiers.org/hco/1/GRCh38#21218235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137691545-C-A

21218239-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691541-G-C

http://identifiers.org/hco/1/GRCh38#21218270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137691513-C-A

21218274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691509-C-T

21218288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691504-T-C

http://identifiers.org/hco/1/GRCh38#21218308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137691493-A-C

http://identifiers.org/hco/1/GRCh38#21218379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137691419-C-A

http://identifiers.org/hco/1/GRCh38#21218409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137691388-C-A

21218409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 137691388-C-T

21218422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 137691375-A-G

21218563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691311-G-A

21218563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691311-G-T

21218933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691210-G-T

21218967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691181-T-C

21218968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691180-G-A

21218968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691180-G-T

http://identifiers.org/hco/1/GRCh38#21218984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137691164-C-A

21218984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691164-C-G

21218984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691164-C-T

21219061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691089-A-G

21219061-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691089-A-T

21219074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691068-G-A

21219074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137691068-G-T

http://identifiers.org/hco/1/GRCh38#21219075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137691067-C-A

http://identifiers.org/hco/1/GRCh38#21219153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137690993-C-A

http://identifiers.org/hco/1/GRCh38#21219189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137690972-C-A

21219251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690911-G-T

21219256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690906-G-A

21219257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690905-T-C

http://identifiers.org/hco/1/GRCh38#21219331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137690840-C-A

21219331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690840-C-T

http://identifiers.org/hco/1/GRCh38#21219353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137690827-C-A

21219353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690827-C-T

21219371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690809-G-C

21219383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690797-G-A

21219383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690797-G-T

21219396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690781-G-C

21219396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690781-G-T

http://identifiers.org/hco/1/GRCh38#21219422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137690755-C-A

21219422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690755-C-T

21219554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690649-T-A

21219554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690649-T-G

21219559-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690643-T-A

21219559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690643-T-G

21219706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690465-G-T

21219710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690461-A-G

21219734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690435-G-T

21219735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690434-G-A

21219735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690434-G-C

21219735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690434-G-T

21219739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 137690430-A-G

http://identifiers.org/hco/1/GRCh38#21219837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137690331-A-C

21219869-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137690305-C-G

21219869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137690305-C-T

21219875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137690299-G-T

21219904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137690267-C-G

21219904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137690267-C-T

21219948-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137690223-T-G

21220079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137690091-T-A

21220132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 137690038-C-T

21220147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137690012-A-G

21220147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137690012-A-T

http://identifiers.org/hco/1/GRCh38#21220200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137689960-A-C

21220200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137689960-A-G

21221157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137689670-G-A

21221693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137689094-A-G

21221719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137689075-G-A

21221727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137689067-T-A

21221727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137689067-T-C

21221757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137689037-C-T

21221850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 137688944-G-A

21221850-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 137688944-G-C

21221877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137688923-C-T

21221900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137688896-A-G

21221937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137688869-G-A

21221937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137688869-G-C

21221937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137688869-G-T

21221938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137688868-G-A

21221938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137688868-G-T

http://identifiers.org/hco/1/GRCh38#21221939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137688867-C-A

21221939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137688867-C-T

http://identifiers.org/hco/1/GRCh38#21221977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137688844-C-A

21222016-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137688809-T-A

21222016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137688809-T-C

21222032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137688793-T-C

21222032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137688793-T-G

21222043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137688782-G-A

21222095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137688730-T-C

http://identifiers.org/hco/1/GRCh38#21222138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137688686-A-C

21222138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137688686-A-G

http://identifiers.org/hco/1/GRCh38#21222156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137688635-C-A

21222226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137688527-C-T

21222386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137688394-G-A

http://identifiers.org/hco/1/GRCh38#21224997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137685707-C-A

21224997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685707-C-T

21225117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685603-T-G

http://identifiers.org/hco/1/GRCh38#21225120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137685600-C-A

21225120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685600-C-T

21225148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685579-G-A

21225148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685579-G-T

21225153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685574-T-C

21225155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685572-C-T

21225362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense variant
orthologous variants: 137685386-T-G

http://identifiers.org/hco/1/GRCh38#21225449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137685299-C-A

21225450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685298-A-G

21225457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685291-G-A

21225491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685274-G-T

21225504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685261-T-C

21225644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685229-G-C

21225714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685163-G-T

21225858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137685081-T-C

21226151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684880-T-C

21226158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684873-G-A

21226160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684871-T-C

21226208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684839-G-A

21226468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684601-T-A

21226491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684585-T-C

21226522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684570-T-G

21227130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684537-G-A

21227130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684537-G-C

21227130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684537-G-T

21227131-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684536-A-T

21227197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense variant
orthologous variants: 137684473-A-T

21227292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684407-T-A

21227320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684395-G-T

http://identifiers.org/hco/1/GRCh38#21227335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137684380-C-A

21227335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684380-C-T

21227402-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684343-G-C

21227431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684313-C-T

21227440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684304-T-C

21227562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684226-G-A

21227783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684027-A-G

http://identifiers.org/hco/1/GRCh38#21227803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137684011-A-C

21227803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684011-A-G

21227803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137684011-A-T

21227855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683970-A-G

21227858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683967-G-A

21227858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683967-G-T

21227859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683966-G-A

21227859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683966-G-T

21227868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683954-G-A

21227868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683954-G-C

21227868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683954-G-T

21227891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683922-G-A

21227891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683922-G-T

21227892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683921-G-A

21227892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683921-G-T

http://identifiers.org/hco/1/GRCh38#21227909-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137683901-A-C

21227909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683901-A-G

21227982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense variant
orthologous variants: 137683826-A-G

21228024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense variant
orthologous variants: 137683784-G-A

21228024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense variant
orthologous variants: 137683784-G-T

http://identifiers.org/hco/1/GRCh38#21228038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137683770-C-A

21228038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: stop gained
orthologous variants: 137683770-C-T

21228088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683721-A-G

21228108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683712-G-A

21228108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683712-G-C

21228108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683712-G-T

21228110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683710-G-A

21228110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683710-G-T

http://identifiers.org/hco/1/GRCh38#21228125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137683695-C-A

21228125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137683695-C-T

21232287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137680215-A-G

http://identifiers.org/hco/1/GRCh38#21232300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137680202-C-A

21232300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, undefined
orthologous variants: 137680202-C-T

21232315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137680187-T-C

21233004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137679387-C-T

http://identifiers.org/hco/1/GRCh38#21233005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137679386-C-A

21233005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137679386-C-T

21233011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137679380-G-T

21233030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137679362-G-T

21233233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679218-T-C

21233233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679218-T-G

21233256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679195-T-C

21233273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679172-T-A

21233273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679172-T-C

21233273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679172-T-G

http://identifiers.org/hco/1/GRCh38#21233291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137679153-C-A

21233291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679153-C-T

21233298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679146-G-A

21233461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679009-G-A

21233461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679009-G-T

21233462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679008-G-A

21233462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679008-G-C

21233462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679008-G-T

21233471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137679000-T-C

21233491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137678980-G-T

21233508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137678946-C-T

21233567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137678901-T-C

http://identifiers.org/hco/1/GRCh38#21233603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137678865-C-A

http://identifiers.org/hco/1/GRCh38#21233672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137678797-A-C

21235668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137677685-C-G

21235714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137677644-A-G

http://identifiers.org/hco/1/GRCh38#21235717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137677641-C-A

http://identifiers.org/hco/1/GRCh38#21235718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137677640-C-A

21235730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137677628-C-T

21235732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137677626-T-A

21235732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137677626-T-C

21235736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137677622-T-C

21235736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137677622-T-G

21235814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137677576-T-C

21235959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137677432-C-T

21236013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137677380-G-A

21236723-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676877-T-A

21236765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137676835-C-T

http://identifiers.org/hco/1/GRCh38#21236810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137676790-A-C

http://identifiers.org/hco/1/GRCh38#21236853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137676748-A-C

21236863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676738-C-T

21236907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676704-A-G

http://identifiers.org/hco/1/GRCh38#21236910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137676701-C-A

http://identifiers.org/hco/1/GRCh38#21236929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137676679-C-A

21236929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676679-C-T

21236967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676669-T-A

21236967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676669-T-C

21236987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676657-G-A

21236987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676657-G-T

21236999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676645-C-T

21237122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676548-G-A

21237151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137676530-G-A

http://identifiers.org/hco/1/GRCh38#21238260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137675837-C-A

21238260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137675837-C-T

21238346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137675736-G-A

http://identifiers.org/hco/1/GRCh38#21238366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137675715-C-A

21238374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137675706-G-A

21238374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137675706-G-T

http://identifiers.org/hco/1/GRCh38#21238390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137675690-C-A

21238390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137675690-C-T

http://identifiers.org/hco/1/GRCh38#21244786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137673975-A-C

21244786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137673975-A-G

21244918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137673847-T-C

21244918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137673847-T-G

21244950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137673759-G-A

21244967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137673700-G-A

21245008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137673659-A-G

21245013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137673654-C-T

21245127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137673541-G-A

21245135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137673533-G-T

21245213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137673493-C-T

21245313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137673397-C-T

21245366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137673345-T-C

http://identifiers.org/hco/1/GRCh38#21245542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137673325-A-C

21245542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137673325-A-G

21245765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137673140-T-A

21245839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137673084-G-A

21247078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137672598-A-G

http://identifiers.org/hco/1/GRCh38#21247156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137672530-C-A

21247156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137672530-C-T

21247199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137672491-A-G

21247199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137672491-A-T

21247476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137672203-T-C

http://identifiers.org/hco/1/GRCh38#21251725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137670166-A-C

21251840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137670049-T-C

21252225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137669731-C-T

21252377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137669591-A-T

21252610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137668294-T-C

http://identifiers.org/hco/1/GRCh38#21252846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137668122-C-A

21252846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137668122-C-T

21254406-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667912-T-G

21254656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667679-C-T

21254689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667646-A-T

21254890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667490-C-T

21255056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667325-G-A

21255247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137667125-C-T

21255318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137667047-G-C

21255574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137666727-T-C

21255574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137666727-T-G

21255575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137666726-G-A

http://identifiers.org/hco/1/GRCh38#21255810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137666245-C-A

21255846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137666211-T-G

21255852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137666205-G-T

21255924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137666140-C-G

21255924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137666140-C-T

21255930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137666134-G-A

21256071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137666000-G-A

http://identifiers.org/hco/1/GRCh38#21256149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137665922-C-A

21256227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665857-G-A

21256227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665857-G-T

21256746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665296-G-A

21256746-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665296-G-C

21256746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665296-G-T

21256786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665254-G-T

21256789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665251-T-A

21256789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665251-T-G

21256822-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665233-T-A

21256822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665233-T-C

http://identifiers.org/hco/1/GRCh38#21256847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137665220-C-A

21256847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665220-C-T

http://identifiers.org/hco/1/GRCh38#21256851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137665216-C-A

21256893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665183-C-T

21257065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665080-C-G

21257071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137665074-G-A

21257181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664988-T-C

21257265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664943-G-A

21257339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664887-T-C

http://identifiers.org/hco/1/GRCh38#21257375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137664849-C-A

http://identifiers.org/hco/1/GRCh38#21257383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137664836-C-A

21257383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664836-C-T

http://identifiers.org/hco/1/GRCh38#21257393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137664813-C-A

21257393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664813-C-T

21257447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664761-C-G

21257497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664731-C-G

21257497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664731-C-T

21257562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137664676-G-A

21257637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664610-G-C

http://identifiers.org/hco/1/GRCh38#21257733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137664549-C-A

21257733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664549-C-T

21257857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664505-T-C

21258393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664189-G-A

http://identifiers.org/hco/1/GRCh38#21258400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137664182-A-C

21258403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137664179-G-A

21258736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137664070-T-A

21258736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137664070-T-C

21258835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137663971-C-T

21259533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137663386-T-C

21259834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137663088-C-T

21259934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137663009-G-A

21260155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662798-T-C

http://identifiers.org/hco/1/GRCh38#21260157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137662796-C-A

21260228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662746-G-T

21260235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662737-G-A

21260247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662725-G-A

21260478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662508-G-A

21260478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662508-G-C

21260498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662484-G-A

21260498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662484-G-T

21260510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662472-G-A

21260510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662472-G-T

21260539-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137662450-T-A

21260705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

21260713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

21260728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

21260871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-G

21262552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137661747-C-T

21265868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137659148-G-A

21265910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137659109-C-G

21265986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137659032-A-G

21266014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137659004-C-T

21266028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137658989-G-T

http://identifiers.org/hco/1/GRCh38#21266112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137658900-C-A

21266112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137658900-C-T

21266123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137658889-G-A

21266123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137658889-G-T

21266281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137658821-T-C

21266329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137658773-C-T

21266379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137658734-A-T

21266388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137658725-G-A

21266395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137658718-G-A

21266396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137658717-G-A

21266396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137658717-G-T

21266397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137658716-A-G

21266595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137658539-A-G

21266613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137658521-G-C

21266616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137658518-A-G

21266689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137658441-G-T

21266869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137658250-T-C

21266906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137658205-G-C

21266906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137658205-G-T

21269106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655976-G-A

21269106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655976-G-C

21269185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655898-C-T

21269195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655888-G-A

21269195-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137655888-G-T

http://identifiers.org/hco/1/GRCh38#21269743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137655423-C-A

21271494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137654682-G-C

21271499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137654677-T-C

21271527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137654649-T-C

21271660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137654485-T-C

http://identifiers.org/hco/1/GRCh38#21272797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137653642-C-A

21272797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137653642-C-G

21272842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137653597-G-A

http://identifiers.org/hco/1/GRCh38#21272899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137653540-A-C

21272905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137653534-G-A

21272905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137653534-G-C

21272919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137653522-G-A

21272919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137653522-G-C

21272933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653508-G-A

21272934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653507-G-A

21272991-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653470-C-G

21272991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653470-C-T

21272994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653467-G-A

21273049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653444-T-A

21273049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653444-T-C

21273049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653444-T-G

21273112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653368-C-G

21273319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653195-G-A

21273333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653185-C-G

21273333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653185-C-T

21273335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653183-G-A

21273339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653179-G-A

21273341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653177-G-A

21273349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653169-G-A

21273364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137653154-T-C

http://identifiers.org/hco/1/GRCh38#21276535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137650856-C-A

21277060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137650672-G-C

21277164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137650570-T-C

21277178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137650553-G-A

21277533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137650170-G-C

21277538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137650165-C-T

21277833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137649858-T-C

21277974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137649681-C-G

21277974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137649681-C-T

21277992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137649663-C-T

21278510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137649193-G-C

21278831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137648930-G-A

21278831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137648930-G-C

21279016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137648746-C-T

21279064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137648604-T-C

21279065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137648603-G-A

21279065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137648603-G-T

21279194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137648468-T-G

21279235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137648427-C-T

http://identifiers.org/hco/1/GRCh38#21279239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137648423-C-A

http://identifiers.org/hco/1/GRCh38#21279260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137648402-C-A

21279314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137648348-G-A

21279314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 137648348-G-C

21279414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 137648248-G-A

21279415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 137648247-C-T

21279443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137648220-C-T

http://identifiers.org/hco/1/GRCh38#21279463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137648199-C-A

21279523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137648139-G-A

http://identifiers.org/hco/1/GRCh38#21279532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137648130-C-A

21279651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137648004-A-G

http://identifiers.org/hco/1/GRCh38#21279718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137647937-C-A

21279718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137647937-C-T

http://identifiers.org/hco/1/GRCh38#21279751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137647904-C-A

http://identifiers.org/hco/1/GRCh38#21279775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137647876-C-A

21279775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137647876-C-T

21279832-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137647830-T-A

21279832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137647830-T-C

21279832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 137647830-T-G

http://identifiers.org/hco/1/GRCh38#21279908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137647768-A-C

21279959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137647726-G-T

21279968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137647717-A-G

21279968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137647717-A-T

21280002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137647682-G-A

21280002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137647682-G-T

21280062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137647615-A-T

21280118-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137647560-C-G

http://identifiers.org/hco/1/GRCh38#21280124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137647554-C-A

21280124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137647554-C-T

21280212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137647451-A-G

21280404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137647258-C-T

21280483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137647208-G-T

http://identifiers.org/hco/1/GRCh38#21283691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137646106-C-A

21283691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137646106-C-G

21283691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137646106-C-T

21283905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137645869-C-T

21283969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137645806-C-T

21284134-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137645680-C-G

21284191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137645634-G-A

21284500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137645383-A-G

21284563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137645322-C-G

21284563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137645322-C-T

21284843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137645055-G-C

21285103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137644812-T-C

21285129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137644793-C-T

21285260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137644722-C-T

http://identifiers.org/hco/1/GRCh38#21285275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137644707-A-C

21285278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137644704-C-G

21285306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137644678-T-A

21285306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137644678-T-C

21285339-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137644656-T-G

21285404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137644593-A-G

21285457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137644523-G-C

21285490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137644492-T-G

21288181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137642540-T-C

http://identifiers.org/hco/1/GRCh38#21288309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137642399-C-A

21289072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137642081-T-A

21289072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137642081-T-C

21289090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137642062-G-A

21289123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137642032-T-C

21289458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641724-C-T

21289465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641717-G-T

21289498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641686-C-T

21289660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641549-G-A

21289720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641474-G-A

21289871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641341-G-A

21290026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137641204-G-A

21290026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137641204-G-C

21290026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137641204-G-T

21290027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137641203-G-A

21290027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137641203-G-T

http://identifiers.org/hco/1/GRCh38#21290030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137641200-C-A

21290030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641200-C-G

21290030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641200-C-T

21290033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641197-G-A

21290033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641197-G-T

21290052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641179-G-A

21290052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641179-G-C

21290052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137641179-G-T

21290220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137641021-A-G

http://identifiers.org/hco/1/GRCh38#21290229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137641016-C-A

21290229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137641016-C-G

21290229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137641016-C-T

http://identifiers.org/hco/1/GRCh38#21290522-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137640845-C-A

21290591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137640770-T-C

21293174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137636945-G-A

21293174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137636945-G-T

21293235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137636889-T-A

21293235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137636889-T-C

http://identifiers.org/hco/1/GRCh38#21293318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137636816-C-A

21293383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137636746-T-C

21293441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137636704-G-A

21293441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137636704-G-T

http://identifiers.org/hco/1/GRCh38#21293454-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137636691-C-A

21293569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 137636594-G-A

21293569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 137636594-G-T

21293714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137636466-G-A

21293714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137636466-G-C

21293714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137636466-G-T

21293901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137636424-T-C

21294062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137636293-A-T

21294071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137636284-T-C

21294142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137636199-T-C

http://identifiers.org/hco/1/GRCh38#21294199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137636145-C-A

http://identifiers.org/hco/1/GRCh38#21294202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137636142-C-A

http://identifiers.org/hco/1/GRCh38#21294238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137636106-C-A

21294238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137636106-C-T

21294386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137635959-G-A

21294386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137635959-G-T

21294425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137635933-G-T

21294458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137635900-A-G

21294495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137635862-A-G

http://identifiers.org/hco/1/GRCh38#21294529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137635830-C-A

21294529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137635830-C-T

21294699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137635674-G-C

21294706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137635667-C-T

21294887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137635489-G-A

21294889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137635487-T-C

21297547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137634258-T-C

http://identifiers.org/hco/1/GRCh38#21297560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137634245-C-A

21297560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137634245-C-T

http://identifiers.org/hco/1/GRCh38#21297575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137634232-A-C

http://identifiers.org/hco/1/GRCh38#21297684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137634140-C-A

21297684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137634140-C-T

21297686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137634138-G-A

21297970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137633866-C-T

21298318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137633552-T-C

21298899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632680-C-T

http://identifiers.org/hco/1/GRCh38#21298931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137632651-C-A

21298931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632651-C-T

21298941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632641-G-T

http://identifiers.org/hco/1/GRCh38#21298975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137632611-C-A

21298975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632611-C-G

21299050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632551-G-A

21299125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 137632477-T-A

21299125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 137632477-T-C

21299211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632395-A-G

21299211-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632395-A-T

21299231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632379-G-A

21299231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632379-G-C

21299231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632379-G-T

21299266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632348-A-G

21299316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632300-T-A

21299323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632293-T-A

21299398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632222-G-T

21299446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632176-G-C

21299446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632176-G-T

21299475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632151-G-A

21299609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 137632047-G-T

21302601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137630546-T-C

21302609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137630538-C-T

21302625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137630525-A-G

21302909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137630289-C-T

21302963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137630266-C-T

21303166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137630097-G-A

21303310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137629984-G-A

21303528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137629776-G-T

21303548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137629755-G-A

21305451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137627956-T-A

21305734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137627712-T-C

21305761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137627685-G-A

21305806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137627619-T-A

21306156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137627266-A-G

21306679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137627013-G-A

http://identifiers.org/hco/1/GRCh38#21306740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137626950-C-A

21306829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137626827-C-T

21307394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137626314-T-A

21307593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137626136-T-G

21307625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137626104-C-G

21307946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137625696-G-A

21308421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137625177-G-A

http://identifiers.org/hco/1/GRCh38#21308422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137625176-A-C

21308443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137625145-G-A

21308482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137625115-G-A

21308648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137624945-C-G

http://identifiers.org/hco/1/GRCh38#21308720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137624889-C-A

21308785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137624833-C-T

21309052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137624554-C-G

21309099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137624494-T-C

21309578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137624061-C-T

21309654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137624014-G-A

21309715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137623966-C-T

http://identifiers.org/hco/1/GRCh38#21309759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137623921-C-A

http://identifiers.org/hco/1/GRCh38#21313132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137620374-C-A

21314002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137619669-C-T

21314107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137619577-C-T

21314654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137619084-C-G

21314654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137619084-C-T

21315240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137618871-T-G

21317403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137617829-A-G

21317497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137617759-G-A

21317528-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137617729-G-C

21317918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137617442-T-C

http://identifiers.org/hco/1/GRCh38#21317929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137617432-C-A

21317929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137617432-C-G

21318020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137617381-G-A

21318249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137617169-G-A

21318274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137617142-A-G

21318600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137616762-C-T

21318799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137616424-G-A

21318799-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137616424-G-C

http://identifiers.org/hco/1/GRCh38#21318802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137616421-C-A

21318802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137616421-C-G

21318802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137616421-C-T

21318895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137616318-T-C

21319002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137616208-T-C

21319067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137616177-A-G

21319250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137616025-T-C

21319289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137616010-G-A

http://identifiers.org/hco/1/GRCh38#21319859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137615402-C-A

21320018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137615285-A-G

21320020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137615283-C-G

21320339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137615153-C-T

21320347-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137615145-T-A

21320647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137614859-G-C

21320732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137614790-G-A

21320767-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137614764-C-G

21320767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137614764-C-T

21321360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137614186-G-A

21321558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137614041-T-G

21321559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137614040-T-C

21321560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137614039-G-A

21322407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137613211-C-G

21322694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137612913-G-A

21323132-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137610189-T-G

21323239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137610082-G-A

21324353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137607415-T-A

21324353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137607415-T-C

21324790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137606974-G-A

21325074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137606723-T-C

21325074-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137606723-T-G

21325081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137606716-G-A

21325480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137606461-T-C

21325707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137606256-A-T

21325729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137606234-C-T

21325790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137606174-G-A

21325816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137606148-G-A

21325909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137606071-C-T

21326137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137605871-C-T

21326261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137605750-G-A

21326379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137605651-C-T

21326514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137605542-T-C

21326514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137605542-T-G

21326579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137605491-T-C

21327088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137605050-T-C

21327136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137604982-A-G

21327164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137604936-C-T

http://identifiers.org/hco/1/GRCh38#21327441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137604664-C-A

21327462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137604636-C-T

21327624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137604516-A-T

21329155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137602797-C-T

21329215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 137602739-A-G

21329321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137602642-G-A

21329321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137602642-G-C

21329417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137602549-C-T

http://identifiers.org/hco/1/GRCh38#21329523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137602444-C-A

21329608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137602370-C-T

21329619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137602359-C-T

21329621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137602357-C-T

21329937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 137602088-A-G

21334347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137598870-C-T

21334433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137598835-A-G

21335139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137598189-G-A

21335275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137598091-A-G

21335288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137598080-C-T

21335423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137597961-T-C

21335605-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137597821-T-G

21335628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137597814-G-A

21335658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137597785-G-C

21335710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137597735-T-C

21335742-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137597709-T-A

21335785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137597660-G-T

21335837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137597562-C-T

21335850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137597518-G-A

21335866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137597501-G-A

21335866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137597501-G-C

21335926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137597415-G-T

21335999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137597345-G-A

21338019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137595437-A-G

21338062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137595393-T-C

21338330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137595164-T-C

21338636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137594933-C-T

21338946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137594669-G-A

21338946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137594669-G-C

21338979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137594633-C-T

21339196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137594475-G-A

21339300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137594390-T-C

http://identifiers.org/hco/1/GRCh38#21341369-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137593559-A-C

21341637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137593368-G-A

21341685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137593320-G-C

21341686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137593319-G-C

21341980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137593149-T-C

21341993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137593136-A-G

21342199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137592922-A-G

21342199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137592922-A-T

21342234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137592884-A-G

21342443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137592680-T-C

21342935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137592266-C-G

21343181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137591991-C-T

21343191-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137591981-A-T

http://identifiers.org/hco/1/GRCh38#21343294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137591895-A-C

21343555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 137591742-C-T

21343688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137591593-G-A

21343688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137591593-G-T

21343691-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137591590-A-G

21343750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137591531-T-G

21343872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137591145-T-G

21343984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137591000-C-T

21344005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137590908-G-C

21344169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137590747-G-A

21344568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137590397-A-T

21344758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137590218-G-A

http://identifiers.org/hco/1/GRCh38#21344906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137590111-C-A

http://identifiers.org/hco/1/GRCh38#21344908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137590109-C-A

21344908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 137590109-C-T

21344970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137590047-T-C

21344970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137590047-T-G

http://identifiers.org/hco/1/GRCh38#21345053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137589972-A-C

21345053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137589972-A-G

21345069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 137589958-A-G

21345145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 137589898-G-A

21345145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 137589898-G-T

21345155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 137589888-G-A

21345238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 137589816-G-A

21345238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 137589816-G-C

21345238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 137589816-G-T

21345241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 137589813-G-A

21345241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 137589813-G-T

http://identifiers.org/hco/1/GRCh38#21345278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137589776-C-A

21345278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137589776-C-G

21345278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137589776-C-T

http://identifiers.org/hco/1/GRCh38#21345286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137589768-A-C

21345286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137589768-A-G

21345286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137589768-A-T

http://identifiers.org/hco/1/GRCh38#21345305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137589755-C-A

21345305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: intron variant
orthologous variants: 137589755-C-T

http://identifiers.org/hco/1/GRCh38#21345440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137589630-C-A

21345440-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 137589630-C-G

21345440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 137589630-C-T

http://identifiers.org/hco/1/GRCh38#21345452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#137589618-C-A

21345452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 137589618-C-G

21345452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 137589618-C-T

http://identifiers.org/hco/1/GRCh38#21345459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#137589611-C-A

21345459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5 prime UTR variant
orthologous variants: 137589611-C-G

21345459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3146
most severe consequence: 5 prime UTR variant
orthologous variants: 137589611-C-T