132410063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28945199-T-A

132410063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 28945199-T-C

132410266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 5 prime UTR variant
orthologous variants: 28945024-T-C

http://identifiers.org/hco/9/GRCh38#132410291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28944999-C-A

132410307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: synonymous_variant, undefined
orthologous variants: 28944983-G-A

132410307-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: synonymous_variant, undefined
orthologous variants: 28944983-G-T

http://identifiers.org/hco/9/GRCh38#132410474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28944816-C-A

132410474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 28944816-C-G

132410474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 28944816-C-T

http://identifiers.org/hco/9/GRCh38#132410475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28944815-C-A

132410475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28944815-C-G

132410475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28944815-C-T

http://identifiers.org/hco/9/GRCh38#132410476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28944811-C-A

http://identifiers.org/hco/9/GRCh38#132410555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28944745-C-A

132410555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28944745-C-T

132410558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28944742-G-A

132410558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28944742-G-C

132410558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28944742-G-T

http://identifiers.org/hco/9/GRCh38#132410733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28944573-C-A

132411074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28944352-G-A

132411074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28944352-G-T

132411135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28944267-G-A

132411135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28944267-G-T

132411196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28944099-A-G

132411225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28944045-G-A

132411235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28944033-T-C

132411286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28943982-G-C

132411286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28943982-G-T

132411317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28943956-G-A

132412060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28943263-C-T

132412097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28943226-A-G

132412414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28942951-T-C

http://identifiers.org/hco/9/GRCh38#132412652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28942790-A-C

132412652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28942790-A-T

132412909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28942566-A-G

132413069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28942424-A-G

132413273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28942171-A-G

132413719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28941743-C-T

132413863-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28941591-T-G

132414306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28941169-C-T

http://identifiers.org/hco/9/GRCh38#132414787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28940760-C-A

132414884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28940668-C-G

132414932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28940620-T-A

132415273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28940317-T-C

132415403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28939593-A-G

132415599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28939423-C-T

132415646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28939375-A-G

132419208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28936190-C-T

132419409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28935997-A-G

132419418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28935990-C-G

132419533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28935898-C-T

132419820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28935523-G-T

132421528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934610-G-T

132421557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934581-G-A

http://identifiers.org/hco/9/GRCh38#132421605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28934539-A-C

132421605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934539-A-G

http://identifiers.org/hco/9/GRCh38#132421706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28934514-C-A

132421706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934514-C-G

http://identifiers.org/hco/9/GRCh38#132421707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28934513-C-A

132421707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934513-C-G

132421707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934513-C-T

http://identifiers.org/hco/9/GRCh38#132421708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28934512-A-C

132421708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934512-A-G

132421708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934512-A-T

132421716-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934504-T-A

132421716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934504-T-C

132421716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934504-T-G

132421760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934491-T-A

132421760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934491-T-C

132421760-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934491-T-G

http://identifiers.org/hco/9/GRCh38#132421777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28934474-C-A

132421777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934474-C-T

132421788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934463-G-A

132421788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28934463-G-T

132422531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28933862-G-A

132422549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28933844-T-C

132422877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28933525-A-T

132422894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28933493-G-A

132422909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28933473-G-T

132423438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28933009-C-T

132423483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28932973-A-G

132423617-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28932855-A-T

132423663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28932804-A-G

132423759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28932053-G-T

132423938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28931917-A-G

132423997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28931855-C-T

132424644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28931582-C-G

132424738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28931485-T-C

132424774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28931460-G-A

132425383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28930856-C-T

http://identifiers.org/hco/9/GRCh38#132426075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28930172-C-A

132426075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28930172-C-G

132426075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28930172-C-T

132426076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28930171-G-A

132426076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28930171-G-C

132426330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28929921-T-C

132426413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28929836-A-T

132426512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28929769-G-A

132427201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28929047-C-T

132434542-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28925249-C-G

132435631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28924257-T-C

132435634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28924254-T-C

132435692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28924222-T-C

132435754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28924156-C-T

132435871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28924090-C-T

132440969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28923565-T-C

132441124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28923461-C-T

132441148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28923437-G-A

http://identifiers.org/hco/9/GRCh38#132441365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28923220-A-C

132441852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28922704-G-T

http://identifiers.org/hco/9/GRCh38#132443686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28920895-C-A

132443767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28920818-G-T

132443843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28920743-C-G

132443949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28920644-G-A

http://identifiers.org/hco/9/GRCh38#132444093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28920500-C-A

132444096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28920497-C-T

132444167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28920443-C-T

132444170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28920440-C-T

132444220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28920398-G-A

http://identifiers.org/hco/9/GRCh38#132444491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28920138-C-A

132444491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28920138-C-T

132444512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28920117-C-T

132452473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28916075-G-A

132452534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28916011-T-G

132452552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28915995-T-C

132452734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28915816-G-A

132452818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28915739-A-G

132452896-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28915661-C-G

132454879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28913301-G-C

132454879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28913301-G-T

132456206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28912322-G-A

132457066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28911626-C-T

132457087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28911605-G-A

132457102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28911598-T-G

http://identifiers.org/hco/9/GRCh38#132457228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28911506-A-C

132457229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28911505-G-A

132457243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28911491-G-A

132457243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28911491-G-T

132458049-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28910105-C-G

132458113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28910050-C-T

132458121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28910035-G-A

http://identifiers.org/hco/9/GRCh38#132458637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28909106-C-A

132458717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28909043-G-A

132458717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28909043-G-T

132458782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28908978-G-A

132459924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28908580-G-A

132460016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28908498-G-A

132460224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28908383-C-G

132460224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28908383-C-T

132460233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28908374-T-C

132460377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28908234-A-G

132460408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28908201-T-C

132460969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28907547-A-G

132460977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28907541-C-G

132461218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28907272-T-G

132461635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28906950-G-A

132462081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28906488-G-A

132462250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28906324-C-T

132463483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28904578-G-C

http://identifiers.org/hco/9/GRCh38#132463583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28904482-C-A

132463598-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28904467-C-G

132463598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28904467-C-T

132469187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28902601-G-A

132474318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28900393-C-T

132474391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28900349-C-T

132474443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28900294-T-C

132474482-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28900265-T-G

132474583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28900165-G-A

132474583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28900165-G-C

132474583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28900165-G-T

132475314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28899511-A-G

132475337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28899489-G-A

132475410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28899419-T-G

132475504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28899331-C-T

132475555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28899280-G-A

132475568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28899270-A-G

132478542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28897000-G-A

132478575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28896972-G-T

132479270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28896322-C-G

132479270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28896322-C-T

132481588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28893967-T-C

132481644-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28893899-G-C

132482193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28893368-T-C

132482194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28893367-T-A

132482198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28893363-T-C

http://identifiers.org/hco/9/GRCh38#132482230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28893331-C-A

132482230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28893331-C-T

132482346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, missense_variant
orthologous variants: 28893242-G-A

132482428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28893196-C-T

http://identifiers.org/hco/9/GRCh38#132482482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28893160-C-A

132482482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28893160-C-T

http://identifiers.org/hco/9/GRCh38#132482491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28893147-C-A

132482491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28893147-C-T

132482509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28893129-G-T

132482563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28893091-T-C

132482573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28893081-A-G

132482574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28893080-C-T

132483435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28891657-G-A

132486478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28887974-C-G

132486865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28887616-G-A

http://identifiers.org/hco/9/GRCh38#132487013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28887460-A-C

132487013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28887460-A-T

132487110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28887366-T-C

132487138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28887338-A-G

132487192-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28887284-T-C

132487961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28886443-T-G

132487992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28886412-G-C

132487992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28886412-G-T

132488297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28886099-C-T

132488323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28886068-T-C

http://identifiers.org/hco/9/GRCh38#132488382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28886019-A-C

132489044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28885579-G-C

132489159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28885388-T-A

132489272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28885280-A-G

http://identifiers.org/hco/9/GRCh38#132489368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28885193-C-A

132489748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28884461-C-T

132489749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28884460-G-A

132489787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28884428-C-T

132494837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28881326-C-T

132494852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28881311-T-C

132494958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28881210-C-T

132495043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28881129-T-G

132495220-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28880999-T-A

http://identifiers.org/hco/9/GRCh38#132495242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28880978-C-A

132495663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28880650-A-G

132495724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28880594-G-A

132495724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28880594-G-T

132495814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28880510-A-G

132495840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28880486-C-T

http://identifiers.org/hco/9/GRCh38#132498688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28875918-C-A

132498688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 28875918-C-T

132498785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: missense variant
orthologous variants: 28875821-G-A

132498788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: missense variant
orthologous variants: 28875818-C-T

132498806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28875800-G-T

132498814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28875763-G-A

http://identifiers.org/hco/9/GRCh38#132498823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28875754-C-A

132498823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28875754-C-T

132498879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28875687-G-A

132498879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28875687-G-T

132499280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28874610-G-A

132499280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28874610-G-T

http://identifiers.org/hco/9/GRCh38#132499349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28874554-C-A

132499349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28874554-C-T

132499407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: missense variant
orthologous variants: 28874496-A-T

132505071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28870316-A-G

132505484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28870006-G-C

132506088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28868969-G-A

132506103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28868954-C-G

132506279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28868781-G-A

132506797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28868103-A-G

132506949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28867966-G-A

132507187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28867407-G-A

132507187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28867407-G-T

http://identifiers.org/hco/9/GRCh38#132507458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28867167-C-A

132507458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28867167-C-T

http://identifiers.org/hco/9/GRCh38#132507880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28866810-A-C

132508013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28866701-A-G

132508074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28866557-G-A

132508084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28866547-A-G

132508084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28866547-A-T

132508248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28866406-T-A

132508460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28866013-G-A

132508461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28866012-G-A

132508466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28866007-G-A

132508590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28865732-G-C

132508590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28865732-G-T

132508706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28865682-A-G

132508900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28865498-G-A

132509065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28865348-A-T

132509238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28865200-G-A

132509276-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28865162-T-A

132509346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28865114-C-T

132509420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28865068-G-A

132510207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28864715-G-A

132510222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28864700-G-C

132514605-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28864339-T-A

132514941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28864033-C-T

132515314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28863562-G-T

132515378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28863475-G-A

132515587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28863283-C-T

132516880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28861528-C-T

132517239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28860834-C-T

132517362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28860706-A-G

132517410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28860658-C-T

132517718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28860359-A-G

132517860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28860203-G-A

132517860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28860203-G-C

132517870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28860193-C-T

132517963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28860096-C-T

132517964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28860095-G-A

132518010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28860044-G-A

132518010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28860044-G-T

132518011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28860043-T-C

132518105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28859956-G-A

132518106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28859955-G-A

132520916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28859653-C-G

132521132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28859491-G-A

132521303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28859357-C-T

132522179-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28858354-T-G

132522296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28858290-G-A

http://identifiers.org/hco/9/GRCh38#132522306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28858280-C-A

132522386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28858199-T-C

132522422-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28858165-G-C

132522477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28858100-T-A

132522703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28857908-C-T

132522715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28857896-G-A

http://identifiers.org/hco/9/GRCh38#132531423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#28856881-C-A

132531529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28856776-G-A

132531544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28856761-A-G

132531618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28856684-T-G

132531631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28856671-G-A

132531631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28856671-G-C

132531631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28856671-G-T

132531632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28856670-G-A

132531632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28856670-G-C

132531632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28856670-G-T

132531976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28856352-G-A

132531976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28856352-G-C

132532255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28856117-G-A

132532255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28856117-G-C

132536722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28853615-C-T

132536742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28853596-C-G

132537210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28853161-G-A

132537371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28853002-C-T

132537374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852999-C-T

132537375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852998-T-G

132537454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852893-A-G

132537454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852893-A-T

http://identifiers.org/hco/9/GRCh38#132537504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28852842-C-A

132537504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852842-C-T

132537516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852832-G-A

132537516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852832-G-T

132537548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852798-G-A

132537548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852798-G-C

http://identifiers.org/hco/9/GRCh38#132537552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28852794-C-A

132537552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852794-C-T

132537813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852567-G-A

132537813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852567-G-T

132537848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852536-G-A

132537848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852536-G-T

132537916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852470-C-T

132538113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852291-T-A

132538113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28852291-T-G

132539579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28850702-G-A

http://identifiers.org/hco/9/GRCh38#132539601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28850679-C-A

132539601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28850679-C-T

132539602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28850678-G-A

132539843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28850529-C-T

132542909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28846141-G-A

132542909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28846141-G-C

http://identifiers.org/hco/9/GRCh38#132543003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28846049-C-A

132543104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28845965-T-C

http://identifiers.org/hco/9/GRCh38#132543134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28845944-C-A

http://identifiers.org/hco/9/GRCh38#132543345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28845416-C-A

132543345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28845416-C-G

132546386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28843293-G-A

132546386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28843293-G-C

http://identifiers.org/hco/9/GRCh38#132546415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28843263-A-C

132546465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28843213-G-A

132546552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28843126-G-A

132546611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28843086-C-T

132546695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron_variant, undefined
orthologous variants: 28843007-C-T

132546711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28842992-A-G

132546896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28842501-T-C

132546972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28842423-G-A

132547173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28842249-A-G

132547195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28842224-T-C

132548759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28840932-T-C

132549158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28840535-C-T

132549389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28840316-C-T

132549493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28840213-C-T

132549873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28840164-T-C

132550046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28840040-G-A

132550055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28840031-C-G

132550055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28840031-C-T

132550098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28839987-G-A

132550438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28838834-A-G

132550438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28838834-A-T

132551768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28838173-T-C

132552075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28837876-T-A

132552316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28837733-G-A

132553187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28837122-C-T

132553200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28837109-C-T

132553221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28837088-C-T

132554177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28836338-G-A

132554656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28836172-C-T

132554809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28836050-G-C

http://identifiers.org/hco/9/GRCh38#132554878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28836002-A-C

132554882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28835998-A-G

132555553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28835428-G-A

132555596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28835385-C-T

http://identifiers.org/hco/9/GRCh38#132555678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28835304-C-A

http://identifiers.org/hco/9/GRCh38#132555913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28835086-C-A

132555913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28835086-C-T

132556002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28835005-A-G

132556026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834981-T-C

132556128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834881-C-G

132556171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834841-T-C

132556220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834798-G-A

132556331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834658-C-T

132556343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834648-G-C

132556364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834627-G-A

132556397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834594-G-A

132556414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834581-G-A

132556419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834576-C-T

132556440-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834553-G-C

132556446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834547-G-A

132556670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834301-C-T

132556932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28834039-T-C

132557157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28833807-G-A

http://identifiers.org/hco/9/GRCh38#132557250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28833714-C-A

132557364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28833614-G-A

132557638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28833233-T-C

132557638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28833233-T-G

http://identifiers.org/hco/9/GRCh38#132557723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28833148-A-C

132560300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28830852-G-A

132560348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28830802-C-T

132561132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28829647-C-T

132561509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28829269-A-G

132561554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28829223-T-A

http://identifiers.org/hco/9/GRCh38#132561556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28829221-A-C

132561678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28829132-C-T

132561684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28829126-T-G

132561706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28829104-G-A

132561769-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28829058-A-G

132561839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28828988-G-T

132561895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28828932-A-G

132565202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28826136-T-C

132565337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28825970-T-C

132565841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28825791-C-G

132565857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28825775-C-T

132566020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28825609-G-A

132566080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28825550-T-C

http://identifiers.org/hco/9/GRCh38#132572117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28818204-C-A

132572117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28818204-C-T

132572249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28818102-A-T

132572293-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28818052-T-A

132572341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: 28818006-A-G

http://identifiers.org/hco/9/GRCh38#132572359-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28817989-A-C

132572439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: synonymous variant
orthologous variants: 28817910-T-C

http://identifiers.org/hco/9/GRCh38#132572469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28817880-C-A

132572469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: missense variant
orthologous variants: 28817880-C-T

132572470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: missense variant
orthologous variants: 28817879-G-A

132572470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: missense variant
orthologous variants: 28817879-G-T

http://identifiers.org/hco/9/GRCh38#132572528-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28817828-A-C

132572528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817828-A-G

132572550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817805-T-C

132572550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817805-T-G

132572551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817804-G-A

132572551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817804-G-T

http://identifiers.org/hco/9/GRCh38#132572573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28817772-C-A

132572606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817725-T-C

http://identifiers.org/hco/9/GRCh38#132572692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28817650-A-C

132572692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817650-A-G

http://identifiers.org/hco/9/GRCh38#132572745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28817527-C-A

132572745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817527-C-T

http://identifiers.org/hco/9/GRCh38#132572764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28817508-C-A

132572764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817508-C-T

132572767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817505-G-A

132572767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817505-G-T

http://identifiers.org/hco/9/GRCh38#132572805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28817468-C-A

132572856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817397-C-T

http://identifiers.org/hco/9/GRCh38#132572857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#28817396-A-C

132572857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817396-A-G

132572865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817388-G-A

132572865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28817388-G-T

132573297-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33776
most severe consequence: 3 prime UTR variant
orthologous variants: 28816978-T-A