62236243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98643213-A-G

62236244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98643214-G-C

62236446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98643412-T-C

62236491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98643457-T-C

62236491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98643457-T-G

http://identifiers.org/hco/1/GRCh38#62236638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98643512-A-C

62236952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98643587-G-T

62236963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98643598-G-A

62237061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98643695-G-A

http://identifiers.org/hco/1/GRCh38#62237150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98643792-C-A

62237150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98643792-C-G

62237150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98643792-C-T

62237230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98643830-T-C

62237268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98643898-G-A

62237268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98643898-G-T

http://identifiers.org/hco/1/GRCh38#62237459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98644083-C-A

62237472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98644096-T-G

62237885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98644343-T-C

62237901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98644359-A-T

62237979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98644437-G-T

62237999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98644457-G-A

62237999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98644457-G-T

62238005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98644463-G-A

62238005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98644463-G-T

62238046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98644504-C-T

http://identifiers.org/hco/1/GRCh38#62238136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#98644578-C-A

62238136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98644578-C-T

http://identifiers.org/hco/1/GRCh38#62238174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98644616-A-C

62238175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98644617-G-T

http://identifiers.org/hco/1/GRCh38#62238198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#98644639-A-C

62238198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98644639-A-G

62238222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98644663-G-T

http://identifiers.org/hco/1/GRCh38#62238230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#98644671-C-A

http://identifiers.org/hco/1/GRCh38#62238256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98644697-C-A

62238256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3 prime UTR variant
orthologous variants: 98644697-C-T

62238274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 98644715-C-T

62238298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: synonymous_variant, undefined
orthologous variants: 98644739-C-T

62238346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: synonymous variant
orthologous variants: 98644787-T-C

http://identifiers.org/hco/1/GRCh38#62238374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98644815-C-A

62238374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: missense variant
orthologous variants: 98644815-C-T

http://identifiers.org/hco/1/GRCh38#62238393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98644830-A-C

http://identifiers.org/hco/1/GRCh38#62238479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98644918-C-A

62238479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98644918-C-T

62238537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98644958-T-A

62239021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98645136-G-A

http://identifiers.org/hco/1/GRCh38#62240828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98646006-C-A

62240828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98646006-C-G

62241573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98646427-G-C

62241669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98646524-T-C

62241723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98646557-G-C

62241723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98646557-G-T

62241876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, undefined
orthologous variants: 98646723-C-G

62241876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, undefined
orthologous variants: 98646723-C-T

62242042-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98646874-G-C

62242146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98646975-G-A

62242146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98646975-G-C

http://identifiers.org/hco/1/GRCh38#62242162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98646991-C-A

62242162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98646991-C-T

62242346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98647084-G-A

62242539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98647219-A-G

62242580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98647298-G-T

62244951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98648275-C-T

62244963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98648287-G-A

62245033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98648352-C-G

62245033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98648352-C-T

62245095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98648416-C-T

62245617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98648857-T-C

62245870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98649026-A-G

62245895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98649050-A-T

62245923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98649066-T-C

62246285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98649233-G-A

62246335-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98649283-G-C

62246335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98649283-G-T

62246388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98649335-G-A

62246389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98649336-A-T

62247237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98649548-T-C

62247483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98649651-G-A

62247835-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98649958-A-T

62247955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98650069-A-T

62247975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98650090-C-T

62248138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98650328-A-G

62248330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98650511-T-C

62249262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98650648-A-G

62252492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98652781-T-C

62252575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98652883-C-T

62252704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98653342-G-C

http://identifiers.org/hco/1/GRCh38#62252802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98653443-C-A

62252984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98653615-T-A

62252984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98653615-T-C

62252985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98653616-G-A

62252985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98653616-G-T

62253030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98653659-C-T

62253094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: synonymous variant
orthologous variants: 98653727-T-C

62253227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98653860-G-T

http://identifiers.org/hco/1/GRCh38#62253265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98653891-C-A

62253866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98654130-G-T

62253977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98654227-C-G

62257513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98655528-G-A

62257647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98655642-C-T

62258127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98656061-C-T

62258619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98656498-C-T

http://identifiers.org/hco/1/GRCh38#62261136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98657434-A-C

http://identifiers.org/hco/1/GRCh38#62261582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98657759-A-C

62261912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98658032-C-T

62261933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98658073-T-C

62261964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98658106-C-T

62262068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98658192-A-G

62262251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98658337-G-C

62262322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98658419-A-G

62263200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 98659601-G-A

62263222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 98659623-G-A

62263222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 98659623-G-T

62263223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 98659624-T-C

62263234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 98659635-G-A

62263263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 98659664-G-A

62263273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 98659674-G-A

62263273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 98659674-G-C

62263273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 98659674-G-T

62263344-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98659742-T-A

62263344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98659742-T-C

62263344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98659742-T-G

62263456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, undefined
orthologous variants: 98659869-G-A

62263465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, undefined
orthologous variants: 98659878-G-T

http://identifiers.org/hco/1/GRCh38#62263476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#98659889-A-C

62264071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98660072-A-G

62264072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98660073-T-A

62264680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98660375-G-A

62264782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98660474-A-G

62265836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98661002-T-C

http://identifiers.org/hco/1/GRCh38#62265842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98661008-C-A

62265843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98661009-T-C

62266089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98661215-C-T

http://identifiers.org/hco/1/GRCh38#62266620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98661540-C-A

62266620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98661540-C-T

62266667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98661577-C-G

62266750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: synonymous variant
orthologous variants: 98661638-G-A

62266750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: synonymous variant
orthologous variants: 98661638-G-T

62266789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: synonymous variant
orthologous variants: 98661677-T-C

62266847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98661732-A-G

62266884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98661763-T-C

62267115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98661944-G-A

62267142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98661973-T-C

62267291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98662097-A-G

62267352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98662156-C-T

62267919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98662544-G-A

62267919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98662544-G-C

62267996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98662619-G-A

62268075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98662692-A-G

62268076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98662693-G-T

http://identifiers.org/hco/1/GRCh38#62268136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98662758-C-A

62268136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98662758-C-G

62268136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98662758-C-T

62268190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98662811-G-T

62268214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98662827-C-T

http://identifiers.org/hco/1/GRCh38#62268234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98662858-C-A

62268234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98662858-C-T

http://identifiers.org/hco/1/GRCh38#62268400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98663024-A-C

http://identifiers.org/hco/1/GRCh38#62268921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: -C-A

62268921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: -C-T

62269031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: -C-T

62271133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98664902-C-T

62271139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98664908-A-G

62271340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98665103-G-C

62271340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98665103-G-T

http://identifiers.org/hco/1/GRCh38#62271351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#98665114-C-A

62271351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, undefined
orthologous variants: 98665114-C-T

62271396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98665157-C-G

62271400-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98665161-C-G

http://identifiers.org/hco/1/GRCh38#62271466-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98665224-A-C

62271604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665364-C-T

62271705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665446-G-A

62271705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665446-G-C

62271705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665446-G-T

62271706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665447-G-A

62271706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665447-G-T

http://identifiers.org/hco/1/GRCh38#62271707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98665448-A-C

62271707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665448-A-G

62271707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665448-A-T

62271714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665458-A-G

62271714-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665458-A-T

62271729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665473-T-C

http://identifiers.org/hco/1/GRCh38#62271762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98665503-C-A

62271762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665503-C-T

http://identifiers.org/hco/1/GRCh38#62271842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98665579-C-A

62271900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665634-G-A

62271900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665634-G-T

62271936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665663-T-A

62271936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665663-T-C

http://identifiers.org/hco/1/GRCh38#62271995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98665717-C-A

62271995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665717-C-T

62272090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98665796-A-G

http://identifiers.org/hco/1/GRCh38#62272103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#98665809-C-A

62272103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98665809-C-T

http://identifiers.org/hco/1/GRCh38#62272148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#98665852-C-A

62272148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98665852-C-G

62272148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98665852-C-T

http://identifiers.org/hco/1/GRCh38#62272219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#98665918-C-A

62272219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 98665918-C-T

62272283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665981-A-G

62272304-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665995-T-A

62272307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665998-T-C

62272307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98665998-T-G

62272383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98666070-T-C

http://identifiers.org/hco/1/GRCh38#62272466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98666148-C-A

http://identifiers.org/hco/1/GRCh38#62272514-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98666201-C-A

62272614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98666289-T-C

62272684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98666343-G-T

http://identifiers.org/hco/1/GRCh38#62272729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98666368-C-A

62272729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98666368-C-T

62272749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98666380-G-T

62272755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98666386-A-G

62272755-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98666386-A-T

http://identifiers.org/hco/1/GRCh38#62273099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98666416-C-A

62273105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98666422-A-G

62273105-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98666422-A-T

62273111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98666429-A-G

62273113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98666431-G-T

62273117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98666435-A-G

62273117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98666435-A-T

62273134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98666453-G-T

62273138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98666457-C-T

62273152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98666471-T-A

62273152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98666471-T-C

62273209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98666506-G-T

62273212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98666509-G-A

62273212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98666509-G-C

62273212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98666509-G-T

62273213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98666531-G-A

62273213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98666531-G-T

62273220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98666538-G-A

62273220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98666538-G-T

62273248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98666572-T-C

62273248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98666572-T-G

62273403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98666727-G-A

62273403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98666727-G-C

62273403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98666727-G-T

http://identifiers.org/hco/1/GRCh38#62273488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98666812-C-A

62273488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98666812-C-T

62273508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98666832-T-A

62273526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98666850-G-A

62273707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98667040-T-C

62273764-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98667097-T-A

62273764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98667097-T-C

62273770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, stop_gained
orthologous variants: 98667103-C-T

62273775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98667108-T-A

http://identifiers.org/hco/1/GRCh38#62273823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98667156-C-A

62273823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98667156-C-T

62273836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98667169-A-G

62273884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98667217-T-C

62273973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98667306-G-C

62274234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98667567-T-C

http://identifiers.org/hco/1/GRCh38#62274255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98667588-C-A

62274255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98667588-C-G

62274255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98667588-C-T

62274261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98667594-G-C

http://identifiers.org/hco/1/GRCh38#62274305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/4/GRCm39#98667638-C-A

62274305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98667638-C-T

62274444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98667774-T-C

62274487-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98667841-G-C

62274554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98667908-G-A

62274554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98667908-G-T

62274570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98667924-T-C

62274600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98667954-C-T

http://identifiers.org/hco/1/GRCh38#62274779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98668121-A-C

62274779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98668121-A-G

62274783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98668125-G-A

62274828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98668170-A-G

62274857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98668199-G-A

62274857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98668199-G-C

62274866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, missense_variant
orthologous variants: 98668208-C-T

62275001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 98668343-A-G

62275167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98668485-G-C

62275167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98668485-G-T

http://identifiers.org/hco/1/GRCh38#62275180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98668498-C-A

62275180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98668498-C-T

62275181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98668499-G-A

62275181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98668499-G-T

http://identifiers.org/hco/1/GRCh38#62275182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98668500-C-A

62275182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98668500-C-T

62275206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98668524-T-C

62275207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98668525-G-T

http://identifiers.org/hco/1/GRCh38#62275210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98668528-C-A

62275210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98668528-C-T

62275211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98668529-T-C

62275228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98668546-T-G

62275239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98668559-G-T

62275675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98668988-T-A

62275738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98669047-G-C

62275739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98669048-T-C

62275836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98669115-G-A

62276005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98669136-A-G

62276031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98669160-C-G

62276080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98669209-T-C

62276151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98669229-T-C

62276248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98669331-T-C

62276530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98669470-C-T

62276538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98669476-G-A

http://identifiers.org/hco/1/GRCh38#62276937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98669846-C-A

62276959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98669864-G-C

62276969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98669874-T-A

62277164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98670059-T-C

62277412-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98670287-T-A

62277484-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98670356-G-C

62277843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98670705-G-A

62277892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98670754-C-T

62277959-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98670826-T-A

62277959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98670826-T-C

62277984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98670848-T-G

62278063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98670936-T-C

62278086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98670957-T-C

62278088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98670959-C-T

62278253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98671227-T-G

62278268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98671244-G-T

http://identifiers.org/hco/1/GRCh38#62278449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98671380-A-C

62278583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98671470-G-A

62278583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98671470-G-C

62278595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98671481-A-G

62278673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98671568-G-A

http://identifiers.org/hco/1/GRCh38#62278784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98671658-C-A

62278784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98671658-C-G

62278946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98671800-A-G

62279025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98671878-C-T

62279089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, undefined
orthologous variants: 98671941-C-G

62279286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, undefined
orthologous variants: 98672491-A-G

62279347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98672538-A-G

62279374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, undefined
orthologous variants: 98672565-G-A

62279374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, undefined
orthologous variants: 98672565-G-C

62280810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673138-T-C

62280814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673142-C-T

62280895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673208-C-T

62280904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673216-G-A

62281015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673348-G-A

62281133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673479-A-G

62281162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673499-C-G

62281193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673530-C-T

62281224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673561-A-G

62281253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673594-G-A

62281254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673595-G-C

62281420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673768-A-G

http://identifiers.org/hco/1/GRCh38#62281422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98673770-C-A

62281433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673781-G-A

62281433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673781-G-T

62281522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673869-C-T

http://identifiers.org/hco/1/GRCh38#62281523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98673870-C-A

62281523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98673870-C-G

62281597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5 prime UTR variant
orthologous variants: 98673941-C-T

62281610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5 prime UTR variant
orthologous variants: 98673954-G-A

62281632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 98673976-G-A

62281632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 98673976-G-C

62281632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, splice_region_variant
orthologous variants: 98673976-G-T

62281660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674001-G-A

62281660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674001-G-T

http://identifiers.org/hco/1/GRCh38#62281719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98674061-A-C

62281719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674061-A-G

http://identifiers.org/hco/1/GRCh38#62281747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98674094-C-A

62281747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674094-C-T

http://identifiers.org/hco/1/GRCh38#62281765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98674109-C-A

62281831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674169-T-C

62281884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674215-G-A

62281917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674249-T-G

62281965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674310-A-G

62281997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674346-G-A

http://identifiers.org/hco/1/GRCh38#62282150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98674463-A-C

62282150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674463-A-G

62282164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674477-T-C

62282391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674678-T-G

62282444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674723-G-A

62282593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674852-G-A

62282631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98674865-G-A

62282967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98675198-A-G

62283154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98675373-T-G

62283240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98675454-C-T

http://identifiers.org/hco/1/GRCh38#62283253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98675465-A-C

http://identifiers.org/hco/1/GRCh38#62283315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98675520-C-A

62283549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98675715-C-T

http://identifiers.org/hco/1/GRCh38#62283766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98675887-C-A

62283768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98675889-T-C

62283828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98675944-A-G

62284200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98676270-T-C

62284333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98676402-G-C

62284333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98676402-G-T

http://identifiers.org/hco/1/GRCh38#62284959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98676883-A-C

62285074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98676977-G-A

62285452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98677649-C-G

62285610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98677809-T-C

62285800-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98677988-T-A

62285853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98678043-C-T

62285991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98678171-C-T

62286223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98678439-T-C

62286958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98679080-G-A

62287097-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98679191-G-C

62287097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 98679191-G-T

62287237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98679318-C-T

62287391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98679450-T-C

62287537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98679598-A-G

62293553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98682446-A-G

62293820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98682831-C-T

62293855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98682865-G-T

62293867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98682877-C-G

62293954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98683026-C-T

http://identifiers.org/hco/1/GRCh38#62294026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98683086-C-A

62294026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98683086-C-T

http://identifiers.org/hco/1/GRCh38#62294068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98683112-A-C

62294169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98683212-T-A

62294191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98683231-C-T

62294196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98683236-A-G

62294286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98683326-A-G

62294353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98683391-C-T

http://identifiers.org/hco/1/GRCh38#62294897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98683908-C-A

62294934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98683945-G-A

62294934-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98683945-G-C

62295023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98684016-A-T

62295176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98684140-T-C

62295186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98684150-G-A

62295186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98684150-G-T

62295192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98684156-G-A

62295487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98684560-A-G

62295508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98684581-T-C

62295602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98684710-G-A

62295642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98684751-C-T

62295752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98684855-C-T

62296064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98685157-G-A

62296250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98685334-A-G

62296319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98685418-T-C

62296361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98685454-C-T

http://identifiers.org/hco/1/GRCh38#62296518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98685608-A-C

62297336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98685748-T-G

62297365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98685774-T-C

http://identifiers.org/hco/1/GRCh38#62297400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98685804-C-A

62297416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98685820-C-T

62297621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98686225-C-T

62297655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98686259-A-G

62297693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98686298-A-G

62297770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98686355-A-G

62297856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98686428-G-A

62297960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98686532-T-C

62298033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98686594-G-T

62298068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98686626-C-T

62299793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98689092-A-T

62300048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron_variant, undefined
orthologous variants: 98689334-T-C

62300239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98689455-G-A

62300357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98689533-A-G

62300574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98689736-A-G

62300729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98689829-C-G

62300773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98689846-G-A

62300875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98689954-C-G

62301068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98690184-G-A

62302562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691222-G-T

62302602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691255-C-T

62302747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691399-C-G

62302840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691489-G-A

62302892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691540-G-C

62303021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691664-G-A

62303072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691718-A-G

62303079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691724-G-A

62303088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691733-G-C

62303152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691796-G-A

62303155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691799-A-G

62303157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691801-T-C

62303203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691854-T-C

62303204-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98691855-G-C

62303368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98692003-G-A

62303438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98692062-A-T

62303440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98692064-G-A

62303448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98692072-G-C

62303840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98692391-C-G

62304494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98692736-C-G

62304555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98692837-G-T

62304577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98692860-G-T

62304599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98692876-G-C

62304659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98692929-T-G

62304938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98693400-G-A

62305688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98694011-G-C

62305727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98694054-G-A

62305728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98694055-A-G

62305793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98694118-T-C

62306554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98694609-G-T

62307551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98694840-G-A

62307553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98694842-G-C

62307898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98695230-G-C

62307963-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98695303-C-G

62307983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98695319-C-T

62309502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98696836-A-G

62309675-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98697129-T-A

62309686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98697139-T-C

http://identifiers.org/hco/1/GRCh38#62309762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98697197-C-A

62309762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98697197-C-T

62309815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98697229-A-G

62310267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98697685-G-A

62310407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98697839-G-A

62310437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98697868-G-A

62310507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98697960-C-T

62310514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98697967-G-T

62310594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98698048-T-G

62310604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98698058-A-T

62310652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98698109-A-G

62310883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98698334-A-G

62310949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98698556-C-T

http://identifiers.org/hco/1/GRCh38#62310998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98698601-C-A

62311082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98698688-G-A

62311376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98699104-C-T

62311453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98699307-C-T

62311557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98699405-G-A

62311727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98699558-G-A

62312099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98699882-C-T

http://identifiers.org/hco/1/GRCh38#62313307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98700563-A-C

62313810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98701032-T-C

62313917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98701182-T-C

62314367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98701288-G-A

62314369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98701290-A-G

62314820-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98701757-T-A

62314864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98701792-C-G

62314904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98701836-C-T

62314932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98701856-T-C

62314950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98701874-T-C

62315025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98701943-T-C

62315134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98702030-G-T

62315153-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98702043-T-A

62315229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98702118-T-C

62315260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98702143-A-G

62315381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98702253-A-T

62315418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98702289-G-C

62315466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98702335-G-A

62315475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98702342-C-G

62315475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98702342-C-T

62315597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98702467-T-C

62315820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98702661-C-T

62315824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98702665-G-A

62316088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98702882-G-A

http://identifiers.org/hco/1/GRCh38#62316271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98703030-C-A

62316590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703381-G-T

62316747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703504-C-T

62316762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703514-T-G

http://identifiers.org/hco/1/GRCh38#62316800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98703554-C-A

62316826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703597-G-T

62316903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703674-G-C

62316962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703722-T-C

62316972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703732-C-T

62316990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703750-G-C

62317075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703811-G-A

62317111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703840-T-C

62317137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703868-G-A

62317140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703871-A-G

62317174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703905-T-A

62317195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703932-A-T

62317214-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703951-T-C

62317224-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703957-T-A

62317224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98703957-T-C

http://identifiers.org/hco/1/GRCh38#62317270-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98704002-A-C

62317340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704080-T-C

62317460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704157-C-G

62317495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704191-G-C

62317507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704207-C-G

62317535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704235-A-G

http://identifiers.org/hco/1/GRCh38#62317544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98704244-C-A

62317591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704290-G-T

62317685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704386-A-G

62317687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704388-A-G

62317698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704394-A-G

62317842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704530-T-C

62317842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704530-T-G

62317974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704659-G-A

http://identifiers.org/hco/1/GRCh38#62318112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98704802-A-C

http://identifiers.org/hco/1/GRCh38#62318153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98704843-C-A

http://identifiers.org/hco/1/GRCh38#62318242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98704944-C-A

62318242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704944-C-T

62318264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98704965-C-T

http://identifiers.org/hco/1/GRCh38#62318380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98705077-C-A

62318380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98705077-C-T

62318393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98705090-G-A

62318515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98705219-C-T

62318663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98705363-G-A

62318962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98705573-G-A

62318962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98705573-G-T

http://identifiers.org/hco/1/GRCh38#62319013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98705593-C-A

62319013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98705593-C-T

62319050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: intron variant
orthologous variants: 98705630-G-T

62319135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 98705692-G-A

62319135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 98705692-G-T

62319163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 98705712-G-A

62319199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5 prime UTR variant
orthologous variants: 98705781-C-G

62319261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5 prime UTR variant
orthologous variants: 98705839-C-G

62319261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5 prime UTR variant
orthologous variants: 98705839-C-T

62319293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 98705871-G-A

http://identifiers.org/hco/1/GRCh38#62319313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#98705891-C-A

62319313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5 prime UTR variant
orthologous variants: 98705891-C-G

62319313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5 prime UTR variant
orthologous variants: 98705891-C-T

62319315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 98705894-G-A

62319357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5 prime UTR variant
orthologous variants: 98705937-G-A

62319365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5 prime UTR variant
orthologous variants: 98705943-G-A

62319365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5 prime UTR variant
orthologous variants: 98705943-G-T

62319375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 98705952-G-A

62319375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 98705952-G-T

62319396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 98705962-A-T

62319400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27263
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 98705966-G-A